Lesson: Carbon and its Compounds

Question: 1

Carbon exists in the atmosphere in the form of:

(a) Carbon monoxide only

(b) Carbon monoxide in traces and carbon dioxide

(c) Carbon dioxide only

(d) Coal

Solution:

b

Question:2

Which of the following statements are usually correct for carbon compounds?

(i) are good conductors of electricity

(ii) are poor conductors of electricity

(iii) have strong forces of attraction between their molecules

(iv) do not have strong forces of attraction between their molecules

(a) (i) and (iii)

(b) (ii) and (iii)

(c) (i) and (iv)

(d) (ii) and (iv)

Solution:

d

Question:3

A molecule of ammonia ( N H 3 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaamOtaiaadIeapaWaaSbaaSqaa8qa caaIZaaapaqabaaaaa@3E26@  ) has:

(a) Only single bonds

(b) Only double bonds

(c) Only triple bonds

(d) Two double bonds and one single bond

Solution:

a

Question: 4

Buckminsterfullerene is an allotropic form of:

(a) Phosphorus

(b) Sulphur

(c) Carbon

(d) Tin

Solution:

c

Question: 5

Which of the following are correct structural isomers of butane?

 

(a) (i) and (iii)

(b) (ii) and (iv)

(c) (i) and (ii)

(d) (iii) and (iv)

Solution:

c

Question:6

CH 3 COOH Heat  +Alkaline KMnO 4   CH 3 COOH MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garuatP5wD4bctPjwzYrxAUvgarmWu51MyVXgaruWq VvNCPvMCG4uz3bqefqvATv2CG4uz3bIuV1wyUbqee0evGueE0jxyai baieYlh91rFfeu0dXdh9vqqj=hEeeu0xXdbba9frFj0=OqFfea0dXd d9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr0=vqpW qaaiaacaWaamaadaGabiaaeaqbayaaaOqaaabaaaaaaaaapeGaae4q aiaabIeapaWaaSbaaSqaa8qacaqGZaaapaqabaGcpeGaae4qaiaab+ eacaqGpbGaaeisaiaaykW7caaMc8+aa4ajaSqaaiaabIeacaqGLbGa aeyyaiaabshacaqGGcGaaGPaVlaaykW7caqGRaGaaeyqaiaabYgaca qGRbGaaeyyaiaabYgacaqGPbGaaeOBaiaabwgacaqGGcGaae4saiaa b2eacaqGUbGaae4ta8aadaWgaaadbaWdbiaabsdacaqGGcGaaeiOaa WdaeqaaaWcpeqabOGaayPKHaGaaGPaVlaaboeacaqGibWdamaaBaaa leaapeGaae4maaWdaeqaaOWdbiaaboeacaqGpbGaae4taiaabIeaaa a@6B4C@  

In the above given reaction, alkaline KMn O 4 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4saiaad2eacaWGUbGaam4ta8aa daWgaaWcbaWdbiaaisdaa8aabeaaaaa@3FF0@  acts as:

(a) Reducing agent

(b) Oxidising agent

(c) Catalyst

(d) Dehydrating agent

Solution:

b

Question:7

Oils on treating with hydrogen in the presence of palladium or nickel catalyst form fats.

This is an example of:

(a) Addition reaction

(b) Substitution reaction

(c) Displacement reaction

(d) Oxidation reaction

Solution:

a

Question: 8

In which of the following compounds, MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabiGaciaacaqabeaada abauaaaOqaaGabaKqzagaeaaaaaaaaa8qacaWFuacaaa@3D55@ OH is the functional group?

(a) Butanone

(b) Butanol

(c) Butanoic acid

(d) Butanal

Solution:

b

Question: 9

The soap molecule has a:

(a) Hydrophilic head and a hydrophobic tail

(b) Hydrophobic head and a hydrophilic tail

(c) Hydrophobic head and a hydrophobic tail

(d) Hydrophilic head and a hydrophilic tail

Solution:

a

Question: 10

Which of the following is the correct representation of electron dot structure of nitrogen?

Solution:

d

Question: 11

Structural formula of ethyne is:

Solution:

a

Question: 12

Identify the unsaturated compounds from the following:

(i) Propane

(ii) Propene

(iii) Propyne

(iv) Chloropropane

(a) (i) and (ii)

(b) (ii) and (iv)

(c) (iii) and (iv)

(d) (ii) and (iii)

Solution:

d

Question: 13

Chlorine reacts with saturated hydrocarbons at room temperature in the:

(a) Absence of sunlight

(b) Presence of sunlight

(c) Presence of water

(d) Presence of hydrochloric acid

Solution:

b

Question: 14

In the soap micelles:

(a) The ionic end of soap is on the surface of the cluster while the carbon chain is in the interior of the cluster.

(b) Ionic end of soap is in the interior of the cluster and the carbon chain is out of the cluster.

(c) Both ionic end and carbon chain are in the interior of the cluster

(d) Both ionic end and carbon chain are on the exterior of the cluster

Solution:

a

Question: 15

Pentane has the molecular formula C 5 H 12 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaiwda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGymaiaaikdaa8aabe aaaaa@4008@ . It has:

(a) 5 covalent bonds

(b) 12 covalent bonds

(c) 16 covalent bonds

(d) 17 covalent bonds

Solution:

Question: 16

Structural formula of benzene is:

Solution:

Question: 17

Ethanol reacts with sodium and forms two products.

These are:

(a) Sodium ethanoate and hydrogen

(b) Sodium ethanoate and oxygen

(c) Sodium ethoxide and hydrogen

(d) Sodium ethoxide and oxygen

Solution:

c

Question: 18

The correct structural formula of butanoic acid is:

Solution:

Question: 19

Vinegar is a solution of:

(a) 50%60% MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlf9irVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaaGynaiaaicdacaGGLaGaai4eGiaa iAdacaaIWaGaaiyjaaaa@4099@  acetic acid in alcohol

(b) 5%8% MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlf9irVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaaGynaiaacwcacaGGtaIaaGioaiaa cwcaaaa@3F27@  acetic acid in alcohol

(c) 5%8% MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlf9irVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaaGynaiaacwcacaGGtaIaaGioaiaa cwcaaaa@3F27@  acetic acid in water

(d) 50%60% MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlf9irVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaaGynaiaaicdacaGGLaGaai4eGiaa iAdacaaIWaGaaiyjaaaa@4099@  acetic acid in water

Solution:

c

Question: 20

Mineral acids are stronger acids than carboxylic acids because

(i) Mineral acids are completely ionised

(ii) Carboxylic acids are completely ionised

(iii) Mineral acids are partially ionised

(iv) Carboxylic acids are partially ionised

(a) (i) and (iv)

(b) (ii) and (iii)

(c) (i) and (ii)

(d) (iii) and (iv)

Solution:

a

Question: 21

Carbon forms four covalent bonds by sharing its four valence electrons with four univalent atoms, e.g. hydrogen. After the formation of four bonds, carbon attains the electronic configuration of:

(a) Helium

(b) Neon

(c) Argon

(d) Krypton

Solution:

b

Question: 22

The correct electron dot structure of a water molecule is:

Solution:

c

Question: 23

Which of the following is not a straight chain hydrocarbon?

Solution:

d

Question; 24

Which among the following are unsaturated hydrocarbons?

 

(a) (i) and (iii)

(b) (ii) and (iii)

(c) (ii) and (iv)

(d) (iii) and (iv)

Solution:

c

Question: 25

Which of the following does not belong to the same homologous series?

(a) C H 4 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaadIeapaWaaSbaaSqaa8qa caaI0aaapaqabaaaaa@3E1C@

(b) C 2 H 6 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGOnaaWdaeqaaaaa@3F4E@

(c) C 3 H 8 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaioda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGioaaWdaeqaaaaa@3F51@

(d) C 4 H 8 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaisda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGioaaWdaeqaaaaa@3F52@

Solution:

d

Question: 26

The name of the compound C H 3 C H 2 CHO MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaadIeapaWaaSbaaSqaa8qa caaIZaaapaqabaGcpeGaaiifGiaadoeacaWGibWdamaaBaaaleaape GaaGOmaaWdaeqaaOWdbiaacsbicaWGdbGaamisaiaad+eaaaa@44D3@  is:

(a) Propanal

(b) Propanone

(c) Ethanol

(d) Ethanal

Solution:

a

Question: 27

The heteroatoms present in C H 3 C H 2 OC H 2 C H 2 Cl MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaadIeapaWaaSbaaSqaa8qa caaIZaaapaqabaGcpeGaaiifGiaadoeacaWGibWdamaaBaaaleaape GaaGOmaaWdaeqaaOWdbiaacsbicaWGpbGaaiifGiaadoeacaWGibWd amaaBaaaleaapeGaaGOmaaWdaeqaaOWdbiaacsbicaWGdbGaamisa8 aadaWgaaWcbaWdbiaaikdaa8aabeaak8qacaWGdbGaamiBaaaa@4BF1@  are:

(i) Oxygen

(ii) Carbon

(iii) Hydrogen

(iv) Chlorine

(a) (i) and (ii)

(b) (ii) and (iii)

(c) (iii) and (iv)

(d) (i) and (iv)

Solution:

d

Question: 28

Which of the following represents saponification reaction?

(a) C H 3 COONa+NaOH CaO C H 4 +N a 2 C O 3 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garuatP5wD4bctPjwzYrxAUvgarmWu51MyVXgaruWq VvNCPvMCG4uz3bqefqvATv2CG4uz3bIuV1wyUbqee0evGueE0jxyai baieYlh91rFfeu0dXdh9vqqj=hEeeu0xXdbba9frFj0=OqFfea0dXd d9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr0=vqpW qaaiaacaWaamaadaGabiaaeaqbayaaaOqaaabaaaaaaaaapeGaam4q aiaadIeapaWaaSbaaSqaa8qacaaIZaaapaqabaGcpeGaam4qaiaad+ eacaWGpbGaamOtaiaadggacqGHRaWkcaWGobGaamyyaiaad+eacaWG ibGaaGPaVlaaykW7daahaaWcbeqaamaaoqcameaacaWGdbGaamyyai aad+eaaeqaliaawkziaaaakiaaykW7caWGdbGaamisa8aadaWgaaWc baWdbiaaisdaa8aabeaak8qacqGHRaWkcaWGobGaamyya8aadaWgaa WcbaWdbiaaikdaa8aabeaak8qacaWGdbGaam4ta8aadaWgaaWcbaWd biaaiodaa8aabeaaaaa@5EF2@

(b) C H 3 COOH+ C 2 H 5 OH H 2 S O 4 C H 3 COO C 2 H 5 + H 2 O MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garuatP5wD4bctPjwzYrxAUvgarmWu51MyVXgaruWq VvNCPvMCG4uz3bqefqvATv2CG4uz3bIuV1wyUbqee0evGueE0jxyai baieYlh91rFfeu0dXdh9vqqj=hEeeu0xXdbba9frFj0=OqFfea0dXd d9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr0=vqpW qaaiaacaWaamaadaGabiaaeaqbayaaaOqaaabaaaaaaaaapeGaam4q aiaadIeapaWaaSbaaSqaa8qacaaIZaaapaqabaGcpeGaam4qaiaad+ eacaWGpbGaamisaiabgUcaRiaadoeapaWaaSbaaSqaa8qacaaIYaaa paqabaGcpeGaamisa8aadaWgaaWcbaWdbiaaiwdaa8aabeaak8qaca WGpbGaamisaiaaykW7caaMc8+aaWbaaSqabeaadaGdKaadbaGaamis amaaBaaabaGaaGOmaaqabaGaam4uaiaad+eadaWgaaqaaiaaisdaae qaaaqabSGaayPKHaaaaOGaaGPaVlaadoeacaWGibWdamaaBaaaleaa peGaaG4maaWdaeqaaOWdbiabgkHiTiaadoeacaWGpbGaam4taiabgk HiTiaadoeapaWaaSbaaSqaa8qacaaIYaaapaqabaGcpeGaamisa8aa daWgaaWcbaWdbiaaiwdaa8aabeaak8qacqGHRaWkcaWGibWdamaaBa aaleaapeGaaGOmaaWdaeqaaOWdbiaad+eaaaa@676E@

(c) 2C H 3 COOH+2Na 2C H 3 COONa+ H 2 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaaGOmaiaaykW7caWGdbGaamisa8aa daWgaaWcbaWdbiaaiodaa8aabeaak8qacaWGdbGaam4taiaad+eaca WGibGaey4kaSIaaGOmaiaaykW7caWGobGaamyyaiaabccacqGHsgIR caaIYaGaaGPaVlaadoeacaWGibWdamaaBaaaleaapeGaaG4maaWdae qaaOWdbiaadoeacaWGpbGaam4taiaad6eacaWGHbGaey4kaSIaamis a8aadaWgaaWcbaWdbiaaikdaa8aabeaaaaa@5759@

(d) C H 3 COO C 2 H 5 +NaOHC H 3 COONa+ C 2 H 5 OH MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaadIeapaWaaSbaaSqaa8qa caaIZaaapaqabaGcpeGaam4qaiaad+eacaWGpbGaam4qa8aadaWgaa WcbaWdbiaaikdaa8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGyn aaWdaeqaaOWdbiabgUcaRiaad6eacaWGHbGaam4taiaadIeacqGHsg IRcaWGdbGaamisa8aadaWgaaWcbaWdbiaaiodaa8aabeaak8qacaWG dbGaam4taiaad+eacaWGobGaamyyaiabgUcaRiaadoeapaWaaSbaaS qaa8qacaaIYaaapaqabaGcpeGaamisa8aadaWgaaWcbaWdbiaaiwda a8aabeaak8qacaWGpbGaamisaaaa@5863@

Solution:

d

Question: 29

The first member of alkyne homologous series is:

(a) Ethyne

(b) Ethene

(c) Propyne

(d) Methane

Solution:

a

Question: 30

Draw the electron dot structure of ethyne and also draw its structural formula:

Solution:

Structural formula of ethyne

H         C          C         H

Electron dot structure of ethyne ( C 2 H 2 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGOmaaWdaeqaaaaa@3F4A@  )

Question: 31

Write the names of the following compounds:

Solution:

(a) Pentanoic acid

(b) Butyne

(c) Heptanal

(d) Pentanol

Question: 32

Identify and name the functional groups present in the following compounds.

Solution:

Question: 33

A compound X is formed by the reaction of a carboxylic acid C 2 H 4 O 2 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGinaaWdaeqaaOWdbi aad+eapaWaaSbaaSqaa8qacaaIYaaapaqabaaaaa@4150@  and an alcohol in presence of a few drops of H 2 S O 4 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaamisa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGtbGaam4ta8aadaWgaaWcbaWdbiaaisdaa8aabe aaaaa@4030@ . The alcohol on oxidation with alkaline KMn O 4 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4saiaad2eacaWGUbGaam4ta8aa daWgaaWcbaWdbiaaisdaa8aabeaaaaa@3FF0@  followed by acidification gives the same carboxylic acid as used in this reaction. Give the names and structures of (a) carboxylic acid, (b) alcohol and (c) the compound X. Also, write the reaction.

Solution:

(a) The carboxylic acid is ethanoic acid.

(b) The alcohol is ethanol.

(c) X is ethyl ethanoate.

The reaction is as follows:

C H 3 COOH+ C 2 H 5 OH  H 2 SO C H 3 COO C 2 H 5 + H 2 O Ethanoic acid  Ethanol            Ethyl ethanoate MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garuatP5wD4bctPjwzYrxAUvgarmWu51MyVXgaruWq VvNCPvMCG4uz3bqefqvATv2CG4uz3bIuV1wyUbqee0evGueE0jxyai baieYlh91rFfeu0dXdh9vqqj=hEeeu0xXdbba9frFj0=OqFfea0dXd d9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr0=vqpW qaaiaacaWaamaadaGabiaaeaqbayaaaOabaeqabaaeaaaaaaaaa8qa caWGdbGaamisa8aadaWgaaWcbaWdbiaaiodaa8aabeaak8qacaWGdb Gaam4taiaad+eacaWGibGaey4kaSIaam4qa8aadaWgaaWcbaWdbiaa ikdaa8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGynaaWdaeqaaO Wdbiaad+eacaWGibGaaiiOaiaaykW7daahaaWcbeqaamaaoqcameaa caqGibWdamaaBaaabaWdbiaabkdaa8aabeaapeGaae4uaiaab+eapa WaaSbaaeaapeGaaeinaiaabckaa8aabeaaa8qabeWccaGLsgcaaaGc caaMc8Uaam4qaiaadIeapaWaaSbaaSqaa8qacaaIZaaapaqabaGcpe Gaam4qaiaad+eacaWGpbGaam4qa8aadaWgaaWcbaWdbiaaikdaa8aa beaak8qacaWGibWdamaaBaaaleaapeGaaGynaaWdaeqaaOWdbiabgU caRiaadIeapaWaaSbaaSqaa8qacaaIYaaapaqabaGcpeGaam4taaqa eamacaWGfbGaamiDaiaadIgacaWGHbGaamOBaiaad+gacaWGPbGaam 4yaiaabccacaWGHbGaam4yaiaadMgacaWGKbGaaiiOaiaacckacaWG fbGaamiDaiaadIgacaWGHbGaamOBaiaad+gacaWGSbGaaiiOaiaacc kacaGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiO aiaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaiiOaiaacckacaaMc8 UaaGPaVlaaykW7caWGfbGaamiDaiaadIgacaWG5bGaamiBaiaabcca caWGLbGaamiDaiaadIgacaWGHbGaamOBaiaad+gacaWGHbGaamiDai aadwgaaaaa@A384@  

Question: 34

Why detergents are better cleansing agents than soaps? Explain.

Solution:

Detergents are better cleansing agents than soaps. This is because detergents are effective even in hard water whereas, soaps cannot be used in hard water for washing clothes or cleaning dirt. This is because the charged ends of detergents do not react with calcium and magnesium ions in hard water to form insoluble precipitate.

Question: 35

Name the functional groups present in the following compounds

(a) C H 3 COC H 2 C H 2 C H 2 C H 3 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaadIeapaWaaSbaaSqaa8qa caaIZaaapaqabaGcpeGaam4qaiaad+eacaWGdbGaamisa8aadaWgaa WcbaWdbiaaikdaa8aabeaak8qacaWGdbGaamisa8aadaWgaaWcbaWd biaaikdaa8aabeaak8qacaWGdbGaamisa8aadaWgaaWcbaWdbiaaik daa8aabeaak8qacaWGdbGaamisa8aadaWgaaWcbaWdbiaaiodaa8aa beaaaaa@4ACC@

(b) C H 3 C H 2 C H 2 COOH MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaadIeapaWaaSbaaSqaa8qa caaIZaaapaqabaGcpeGaam4qaiaadIeapaWaaSbaaSqaa8qacaaIYa aapaqabaGcpeGaam4qaiaadIeapaWaaSbaaSqaa8qacaaIYaaapaqa baGcpeGaam4qaiaad+eacaWGpbGaamisaaaa@46FC@

(c) C H 3 C H 2 C H 2 C H 2 CHO MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaadIeapaWaaSbaaSqaa8qa caaIZaaapaqabaGcpeGaam4qaiaadIeapaWaaSbaaSqaa8qacaaIYa aapaqabaGcpeGaam4qaiaadIeapaWaaSbaaSqaa8qacaaIYaaapaqa baGcpeGaam4qaiaadIeapaWaaSbaaSqaa8qacaaIYaaapaqabaGcpe Gaam4qaiaadIeacaWGpbaaaa@48ED@

(d) C H 3 C H 2 OH MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaadIeapaWaaSbaaSqaa8qa caaIZaaapaqabaGcpeGaam4qaiaadIeapaWaaSbaaSqaa8qacaaIYa aapaqabaGcpeGaam4taiaadIeaaaa@429B@

Solution:

(a) Ketone

(b) Carboxylic acid

(c) Aldehyde

(d) Alcohol

Question: 36

How is ethene prepared from ethanol? Give the reaction involved in it.

Solution:

Ethanol dehydrates on heating with concentrated sulphuric acid at 443 K and gives ethane and water.

C 2 H 5 OH 443K Hotconc. H 2 S O 4 C H 2 =C H 2 + H 2 O MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garuatP5wD4bctPjwzYrxAUvgarmWu51MyVXgaruWq VvNCPvMCG4uz3bqefqvATv2CG4uz3bIuV1wyUbqee0evGueE0jxyai baieYlh91rFfeu0dXdh9vqqj=hEeeu0xXdbba9frFj0=OqFfea0dXd d9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr0=vqpW qaaiaacaWaamaadaGabiaaeaqbayaaaOqaaiaadoeadaWgaaWcbaGa aGOmaaqabaGccaWGibWaaSbaaSqaaiaaiwdaaeqaaOGaam4taiaadI eacaaMc8+aa4alaSqaaiaadIeacaWGVbGaamiDaiaaykW7caaMc8Ua am4yaiaad+gacaWGUbGaam4yaiaaykW7caGGUaGaaGPaVlaaykW7ca WGibWaaSbaaWqaaiaaikdaaeqaaSGaam4uaiaad+eadaWgaaadbaGa aGinaaqabaaaleaacaaI0aGaaGinaiaaiodacaaMc8UaaGPaVlaadU eaaOGaayPKHaGaaGPaVlaaykW7caWGdbGaamisamaaBaaaleaacaaI Yaaabeaakiabg2da9iaadoeacaWGibWaaSbaaSqaaiaaikdaaeqaaO Gaey4kaSIaamisamaaBaaaleaacaaIYaaabeaakiaad+eaaaa@6FB0@  

Question: 37

Intake of small quantity of methanol can be lethal. Give comment.

Solution:

Methanol gets oxidised in the liver and forms methanal. Methanal reacts rapidly with the protoplasm and leads to its coagulation. It also blocks the optic nerves leading to blindness.

Question: 38

A gas is evolved when ethanol reacts with sodium. Name the gas evolved and also write the balanced chemical equation of the reaction involved.

Solution:

Hydrogen gas is evolved when ethanol reacts with sodium. The equation for the reaction is:

2C H 3 C H 2 OH+2Na2C H 3 C H 2 ONa+ H 2 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaaGOmaiaaykW7caWGdbGaamisa8aa daWgaaWcbaWdbiaaiodaa8aabeaak8qacaWGdbGaamisa8aadaWgaa WcbaWdbiaaikdaa8aabeaak8qacaWGpbGaamisaiabgUcaRiaaikda caaMc8UaamOtaiaadggacqGHsgIRcaaIYaGaaGPaVlaadoeacaWGib WdamaaBaaaleaapeGaaG4maaWdaeqaaOWdbiaadoeacaWGibWdamaa BaaaleaapeGaaGOmaaWdaeqaaOWdbiaad+eacaWGobGaamyyaiabgU caRiaadIeapaWaaSbaaSqaa8qacaaIYaaapaqabaaaaa@58D5@

Question: 39

Ethene is formed when ethanol at 443 K is heated with excess of concentrated sulphuric acid. What is the role of sulphuric acid in this reaction? Write the balanced chemical equation of this reaction.

Solution:

When ethanol is heated to form ethane, sulphuric acid acts as a dehydrating agent in the reaction.

C 2 H 5 OH 443K Hotconc. H 2 S O 4 C H 2 =C H 2 + H 2 O MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garuatP5wD4bctPjwzYrxAUvgarmWu51MyVXgaruWq VvNCPvMCG4uz3bqefqvATv2CG4uz3bIuV1wyUbqee0evGueE0jxyai baieYlh91rFfeu0dXdh9vqqj=hEeeu0xXdbba9frFj0=OqFfea0dXd d9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr0=vqpW qaaiaacaWaamaadaGabiaaeaqbayaaaOqaaiaadoeadaWgaaWcbaGa aGOmaaqabaGccaWGibWaaSbaaSqaaiaaiwdaaeqaaOGaam4taiaadI eacaaMc8+aa4alaSqaaiaadIeacaWGVbGaamiDaiaaykW7caWGJbGa am4Baiaad6gacaWGJbGaaGPaVlaac6cacaaMc8UaamisamaaBaaame aacaaIYaaabeaaliaadofacaWGpbWaaSbaaWqaaiaaisdaaeqaaaWc baGaaGinaiaaisdacaaIZaGaaGPaVlaaykW7caWGlbaakiaawkziai aaykW7caaMc8Uaam4qaiaadIeadaWgaaWcbaGaaGOmaaqabaGccqGH 9aqpcaWGdbGaamisamaaBaaaleaacaaIYaaabeaakiabgUcaRiaadI eadaWgaaWcbaGaaGOmaaqabaGccaWGpbaaaa@6C9A@  

Question: 40

Carbon, Group (14) element in the Periodic Table, is known to form compounds with many elements.

Write an example of a compound formed with:

(a) Chlorine (Group 17 of Periodic Table)

(b) Oxygen (Group 16 of Periodic Table)

Solution:

(a) Carbon tetrachloride ( CC l 4 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaadoeacaWGSbWdamaaBaaa leaapeGaaGinaaWdaeqaaaaa@3F3B@  )

(b) Carbon dioxide ( C O 2 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh9frVeeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaad+eapaWaaSbaaSqaa8qa caaIYaaapaqabaaaaa@3E21@  )

Question: 41

In electron dot structure, the valence shell electrons are represented by crosses or dots.

(a) The atomic number of chlorine is 17. Write its electronic configuration

(b) Draw the electron dot structure of chlorine molecule.

Solution:

(a) Electronic configuration of chlorine:

 

K

L

M

Number of electrons

2

8

7

Question: 42

Catenation is the ability of an atom to form bonds with other atoms of the same element. It is exhibited by both carbon and silicon. Compare the ability of catenation of the two elements. Give reasons.

Solution:

Carbon has a smaller size. Due to its smaller size, carbon exhibits catenation much more than silicon, which has a relatively bigger size. This smaller size makes the C MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabiGaciaacaqabeaada abauaaaOqaaGabaKqzagaeaaaaaaaaa8qacaWFtacaaa@3D54@ C bonds strong while the Si MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabiGaciaacaqabeaada abauaaaOqaaGabaKqzagaeaaaaaaaaa8qacaWFtacaaa@3D54@ Si bonds are comparatively weaker.

Question: 43

Unsaturated hydrocarbons contain multiple bonds between the two C-atoms and show addition reactions. Give the test to distinguish ethane from ethene.

Solution:

Unsaturated hydrocarbons have double or triple bonds between two carbon atoms. They participate in the addition reaction.

Due to the presence of double bond, these molecules can break one of the carbon-carbon bonds and can add other atoms by sharing of electrons with new atoms.

Thus, addition reaction results in the formation of a saturated compound.

All unsaturated carbon compounds decolorize bromine water whereas all saturated hydrocarbons do not decolorize bromine water.

Ethane and ethene can, thus, be distinguished by the bromine water test.

Question: 44

Match the reactions given in Column (A) with the names given in column (B).

Solution:

(a) MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabiGaciaacaqabeaada abauaaaOqaaGabaKqzagaeaaaaaaaaa8qacaWFuacaaa@3D55@  (iv)

(b) MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabiGaciaacaqabeaada abauaaaOqaaGabaKqzagaeaaaaaaaaa8qacaWFuacaaa@3D55@  (i)

(c) MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabiGaciaacaqabeaada abauaaaOqaaGabaKqzagaeaaaaaaaaa8qacaWFuacaaa@3D55@  (ii)

(d) MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabiGaciaacaqabeaada abauaaaOqaaGabaKqzagaeaaaaaaaaa8qacaWFuacaaa@3D55@  (iii)

Question: 45

Write the structural formulae of all the isomers of hexane.

Solution:

Question: 46

What is the role of metal or reagents written on arrows in the given chemical reactions?

Solution:

(a)  Ni acts as a catalyst.

(b) Concentrated H 2 S O 4 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaamisa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGtbGaam4ta8aadaWgaaWcbaWdbiaaisdaa8aabe aaaaa@4063@  acts as a catalyst.

(c) Alkaline KMn O 4 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4saiaad2eacaWGUbGaam4ta8aa daWgaaWcbaWdbiaaisdaa8aabeaaaaa@4023@  acts as an oxidising agent.

Question: 47

A salt X is formed and a gas is evolved when ethanoic acid reacts with sodium hydrogen carbonate. Name the salt X and the gas evolved. Describe an activity and draw the diagram of the apparatus to prove that the evolved gas is the one which you have named. Also, write chemical equation of the reaction involved.

Solution:

When ethanoic acid reacts with sodium hydrogen carbonate, sodium ethanoate is formed. Thus, X is sodium ethanoate.

Gas evolved is carbon dioxide.

Activity: The gas that is evolved is passed through lime water. It turns the lime water milky. This confirms the evolution of carbon dioxide gas in the reaction.

C H 3 COOH+NaHC O 3 C H 3 COONa+ H 2 O+C O 2 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaadIeapaWaaSbaaSqaa8qa caaIZaaapaqabaGcpeGaam4qaiaad+eacaWGpbGaamisaiabgUcaRi aad6eacaWGHbGaamisaiaadoeacaWGpbWdamaaBaaaleaapeGaaG4m aaWdaeqaaOWdbiabgkziUkaadoeacaWGibWdamaaBaaaleaapeGaaG 4maaWdaeqaaOWdbiaadoeacaWGpbGaam4taiaad6eacaWGHbGaey4k aSIaamisa8aadaWgaaWcbaWdbiaaikdaa8aabeaak8qacaWGpbGaey 4kaSIaam4qaiaad+eapaWaaSbaaSqaa8qacaaIYaaapaqabaaaaa@57FD@

Question: 48

(a) What are hydrocarbons? Give examples.

(b) Give the structural differences between saturated and unsaturated hydrocarbons with two examples each.

(c) What is a functional group? Give examples of four different functional groups.

Solution:

(a)   Hydrocarbons are compounds formed mainly from carbon and hydrogen. E.g. methane, ethene, propyne, butanol. pentanoic acid, etc.

(b)   In saturated hydrocarbons, there is no double or triple bond between two carbon atoms.

In unsaturated hydrocarbons, there is at least one double or triple bond between two carbon atoms.

(c)   Functional group MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabiGaciaacaqabeaada abauaaaOqaaGabaKqzagaeaaaaaaaaa8qacaWFtacaaa@3D54@  A functional group is an atom or a group of atoms joined in a specific manner which is responsible for the characteristic chemical properties of the organic compounds. Examples of functional groups includes hydroxyl group ( MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabiGaciaacaqabeaada abauaaaOqaaGabaKqzagaeaaaaaaaaa8qacaWFtacaaa@3D54@ OH), aldehyde group ( MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabiGaciaacaqabeaada abauaaaOqaaGabaKqzagaeaaaaaaaaa8qacaWFtacaaa@3D54@ CHO), carboxylic group ( MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabiGaciaacaqabeaada abauaaaOqaaGabaKqzagaeaaaaaaaaa8qacaWFtacaaa@3D54@ COOH), etc.

Question: 49

Name the reaction which is commonly used in the conversion of vegetable oils to fats. Explain the reaction involved in detail.

Solution:

The reaction which is commonly used in the conversion of vegetable oils to fats is called hydrogenation reaction.

This reaction involves the addition of hydrogen to an unsaturated hydrocarbon to obtain saturated hydrocarbon. This reaction is carried out in the presence of a catalyst like nickel or palladium.

It can be seen that one of the two bonds between the carbon atoms breaks to accommodate hydrogen and form saturated hydrocarbon.

Question: 50

(a) Write the formula and draw electron dot structure of carbon tetrachloride.

(b) What is saponification? Write the reaction involved in this process.

Solution:

a)      The chemical formula for carbon tetrachloride is CC l 4 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaadoeacaWGSbWdamaaBaaa leaapeGaaGinaaWdaeqaaaaa@3F3B@ .

(b) Saponification is the process of making soap. It involves conversion of ethyl acetate into salts of carboxylic acids and ethanol by treating them with a base.

C H 3 C O 2 O H 5 NaOH C H 3 COONa+ C 2 H 5 OH MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garuatP5wD4bctPjwzYrxAUvgarmWu51MyVXgaruWq VvNCPvMCG4uz3bqefqvATv2CG4uz3bIuV1wyUbqee0evGueE0jxyai baieYlh91rFfeu0dXdh9vqqj=hEeeu0xXdbba9frFj0=OqFfea0dXd d9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr0=vqpW qaaiaacaWaamaadaGabiaaeaqbayaaaOqaaabaaaaaaaaapeGaam4q aiaadIeapaWaaSbaaSqaa8qacaaIZaaapaqabaGcpeGaam4qaiaad+ eadaWgaaWcbaGaaGOmaaqabaGccaWGpbGaamisamaaBaaaleaacaaI 1aaabeaakiaaykW7caaMc8+aa4ajaSqaaiaad6eacaWGHbGaam4tai aadIeaaeqakiaawkziaiaaykW7caaMc8Uaam4qaiaadIeapaWaaSba aSqaa8qacaaIZaaapaqabaGcpeGaam4qaiaad+eacaWGpbGaamOtai aadggacqGHRaWkcaaMc8Uaam4qa8aadaWgaaWcbaWdbiaaikdaa8aa beaakiaadIeapeWaaSbaaSqaaiaaiwdaaeqaaOGaam4taiaadIeaaa a@634D@

Question 51

Esters are sweet-smelling substances and are used in making perfumes. Suggest some activity and the reaction involved for the preparation of an ester with well labelled diagram.

Solution:

Activity

·         Take 1ml of pure ethanol and 1ml ethanoic acid along with a few drops of concentrated sulphuric acid in a test tube.

·         Warm the content in a water-bath at about 60°C MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaaGOnaiaaicdacqGHWcaScaWGdbaa aa@3FD0@  for at least 5 minutes.

·         Pour the content into a beaker that contains 20-50 ml of water and smell the resulting mixture.

Observation: The mixture smells sweet indicating the formation of ester.

The reaction is as follows:

C H 3 COOH+ C 2 H 5 OH H 2 S O 4 C H 3 COO C 2 H 5 + H 2 O Ethanoic acid  Ethanol         Ester ( Ethyl ethanoate ) MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garuatP5wD4bctPjwzYrxAUvgarmWu51MyVXgaruWq VvNCPvMCG4uz3bqefqvATv2CG4uz3bIuV1wyUbqee0evGueE0jxyai baieYlh91rFfeu0dXdh9vqqj=hEeeu0xXdbba9frFj0=OqFfea0dXd d9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr0=vqpW qaaiaacaWaamaadaGabiaaeaqbayaaaOabaeqabaaeaaaaaaaaa8qa caWGdbGaamisa8aadaWgaaWcbaWdbiaaiodaa8aabeaak8qacaWGdb Gaam4taiaad+eacaWGibGaey4kaSIaaGPaVlaaykW7caWGdbWaaSba aSqaaiaaikdaaeqaaOGaamisa8aadaWgaaWcbaWdbiaaiwdaa8aabe aakiaad+eacaWGibWdbmaaoqcaleaacaWGibWaaSbaaWqaaiaaikda aeqaaSGaam4uaiaad+eadaWgaaadbaGaaGinaaqabaaaleqakiaawk ziaiaaykW7caaMc8Uaam4qaiaadIeapaWaaSbaaSqaa8qacaaIZaaa paqabaGcpeGaam4qaiaad+eacaWGpbGaam4qamaaBaaaleaacaaIYa aabeaakiaadIeadaWgaaWcbaGaaGynaaqabaGccqGHRaWkcaaMc8+d aiaadIeapeWaaSbaaSqaaiaaikdaaeqaaOGaam4taaqaaaqaaiaadw eacaWG0bGaamiAaiaadggacaWGUbGaam4BaiaadMgacaWGJbGaaeii aiaadggacaWGJbGaamyAaiaadsgacaGGGcGaaiiOaiaadweacaWG0b GaamiAaiaadggacaWGUbGaam4BaiaadYgacaGGGcGaaiiOaiaaccka caGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaacckacaWGfbGaam4Cai aadshacaWGLbGaamOCaiaabccapaWaaeWaaeaapeGaamyraiaadsha caWGObGaamyEaiaadYgacaqGGaGaamyzaiaadshacaWGObGaamyyai aad6gacaWGVbGaamyyaiaadshacaWGLbaapaGaayjkaiaawMcaaaaa aa@9B01@

Question: 52

A compound C (molecular formula C 2 H 4 O 2 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGinaaWdaeqaaOWdbi aad+eapaWaaSbaaSqaa8qacaaIYaaapaqabaaaaa@4183@  ) reacts with Na MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabiGaciaacaqabeaada abauaaaOqaaGabaKqzagaeaaaaaaaaa8qacaWFtacaaa@3D54@  metal to form a compound R and evolves a gas which burns with a pop sound. Compound C on treatment with an alcohol A in the presence of an acid forms a sweet-smelling compound S (molecular formula C 3 H 6 O 2 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaioda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGOnaaWdaeqaaOWdbi aad+eapaWaaSbaaSqaa8qacaaIYaaapaqabaaaaa@4186@  ). On addition of NaOH to C, it also gives R and water. Son treatment with NaOH solution gives back R and A. Identify C, R, A, S and write down the reactions involved.

Solution:

Here, compound C (molecular formula C 2 H 4 O 2 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGinaaWdaeqaaOWdbi aad+eapaWaaSbaaSqaa8qacaaIYaaapaqabaaaaa@4183@  ) is ethanoic acid.

R is formed when ethanoic acid reacts with sodium. Thus, R is sodium salt of ethanoic acid (sodium acetate) and gas evolved is hydrogen.

On reacting with an alcohol A, ethanoic acid forms a compound S (molecular formula C 3 H 6 O 2 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaioda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGOnaaWdaeqaaOWdbi aad+eapaWaaSbaaSqaa8qacaaIYaaapaqabaaaaa@4186@  ).

Thus, S is an ester (methyl acetate) and alcohol A is methanol.

The reactions are:

(a)   2C H 3 COOH+2Na2C H 3 COONa+ H 2 ( C )                                   ( R ) MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOabaeqabaaeaaaaaaaaa8qacaaIYaGaaGPaVlaadoeacaWG ibWdamaaBaaaleaapeGaaG4maaWdaeqaaOWdbiaadoeacaWGpbGaam 4taiaadIeacqGHRaWkcaaIYaGaaGPaVlaad6eacaWGHbGaeyOKH4Qa aGOmaiaaykW7caWGdbGaamisa8aadaWgaaWcbaWdbiaaiodaa8aabe aak8qacaWGdbGaam4taiaad+eacaWGobGaamyyaiabgUcaRiaadIea paWaaSbaaSqaa8qacaaIYaaapaqabaaakeabadGaaGPaVlaaykW7ca aMc8UaaGPaVlaaykW7caaMc8+aaeWaaeaapeGaam4qaaWdaiaawIca caGLPaaapeGaaiiOaiaacckacaGGGcGaaiiOaiaacckacaaMc8UaaG PaVlaaykW7caaMc8UaaiiOaiaacckacaGGGcGaaiiOaiaacckacaGG GcGaaiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaacc kacaGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiO aiaacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGc WdamaabmaabaWdbiaadkfaa8aacaGLOaGaayzkaaaaaaa@93F3@

(b)   C H 3 COOH+C H 3 OH H 2 S O 4 C H 3 COO C 2 H 5 + H 2 O ( C )         ( A )( S ) MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garuatP5wD4bctPjwzYrxAUvgarmWu51MyVXgaruWq VvNCPvMCG4uz3bqefqvATv2CG4uz3bIuV1wyUbqee0evGueE0jxyai baieYlh91rFfeu0dXdh9vqqj=hEeeu0xXdbba9frFj0=OqFfea0dXd d9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr0=vqpW qaaiaacaWaamaadaGabiaaeaqbayaaaOabaeqabaaeaaaaaaaaa8qa caWGdbGaamisa8aadaWgaaWcbaWdbiaaiodaa8aabeaak8qacaWGdb Gaam4taiaad+eacaWGibGaey4kaSIaaGPaVlaaykW7caWGdbGaamis a8aadaWgaaWcbaWdbiaaiodaa8aabeaak8qacaWGpbGaamisamaaoq caleaaiiGacaWFibWdamaaBaaameaapeGaaGOmaaWdaeqaaSWdbiaa =nfacaWFpbWdamaaBaaameaapeGaaGinaaWdaeqaaaWcpeqabOGaay PKHaGaaGPaVlaaykW7caWGdbGaamisa8aadaWgaaWcbaWdbiaaioda a8aabeaak8qacaWGdbGaam4taiaad+eacaWGdbWaaSbaaSqaaiaaik daaeqaaOGaamisamaaBaaaleaacaaI1aaabeaakiabgUcaRiaaykW7 paGaamisa8qadaWgaaWcbaGaaGOmaaqabaGccaWGpbaabaWdaiaayk W7caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVpaabmaabaWdbiaadoea a8aacaGLOaGaayzkaaWdbiaacckacaGGGcGaaiiOaiaacckacaGGGc GaaiiOaiaacckacaGGGcGaaiiOaiaaykW7caaMc8UaaGPaVlaaykW7 caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVl aaykW7caaMc8UaaGPaV=aadaqadaqaa8qacaWGbbaapaGaayjkaiaa wMcaaiaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7ca aMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaa ykW7caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaG PaVlaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7caaM c8UaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaayk W7caaMc8+aaeWaaeaapeGaam4uaaWdaiaawIcacaGLPaaaaaaa@D8CF@

(c)   C H 3 COOH+NaOHC H 3 COONa+ H 2 O                                                    ( R ) MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOabaeqabaaeaaaaaaaaa8qacaWGdbGaamisa8aadaWgaaWc baWdbiaaiodaa8aabeaak8qacaWGdbGaam4taiaad+eacaWGibGaey 4kaSIaamOtaiaadggacaWGpbGaamisaiabgkziUkaadoeacaWGibWd amaaBaaaleaapeGaaG4maaWdaeqaaOWdbiaadoeacaWGpbGaam4tai aad6eacaWGHbGaey4kaSIaamisa8aadaWgaaWcbaWdbiaaikdaa8aa beaak8qacaWGpbaabqaWaiaacckacaGGGcGaaiiOaiaacckacaGGGc GaaiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaaccka caGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiOai aacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGcGa aiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaacckaca GGGcGaaiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaa cckacaGGGcGaaiiOaiaacckacaGGGcGaaiiOa8aadaqadaqaa8qaca WGsbaapaGaayjkaiaawMcaaaaaaa@8FF5@

(d)   C H 3 COO H 3 +NaOHC H 3 COONa+C H 3 OH                                                      ( R )            ( A ) MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOabaeqabaaeaaaaaaaaa8qacaWGdbGaamisa8aadaWgaaWc baWdbiaaiodaa8aabeaak8qacaWGdbGaam4taiaad+eacaWGibWdam aaBaaaleaapeGaaG4maaWdaeqaaOWdbiabgUcaRiaad6eacaWGHbGa am4taiaadIeacqGHsgIRcaWGdbGaamisa8aadaWgaaWcbaWdbiaaio daa8aabeaak8qacaWGdbGaam4taiaad+eacaWGobGaamyyaiabgUca RiaadoeacaWGibWdamaaBaaaleaapeGaaG4maaWdaeqaaOWdbiaad+ eacaWGibaabqaWaiaacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiO aiaacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGc GaaiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaaccka caGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiOai aacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGcGa aiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaacckaca GGGcGaaiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGcWdamaabmaa baWdbiaadkfaa8aacaGLOaGaayzkaaWdbiaacckacaGGGcGaaiiOai aacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaacckacaGGGcGa aiiOa8aadaqadaqaa8qacaWGbbaapaGaayjkaiaawMcaaaaaaa@A541@

Question: 53

Look at the figure which is given below and answer the following questions.

(a) What change would you observe in the calcium hydroxide solution taken in tube B?

(b) Write the reaction involved in test tubes A and B respectively.

(c) If ethanol is given instead of ethanoic acid, would you expect the same change?

(d) How can a solution of limewater be prepared in the laboratory?

Solution:

(a)   Calcium hydroxide solution will turn milky when the gas evolved in the reaction is passed through it.

(b) Reactions involved in test tube A

2C H 3 COOH+N a 2 C O 3 2C H 3 COONa+ H 2 O+C O 2 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaaGOmaiaaykW7caWGdbGaamisa8aa daWgaaWcbaWdbiaaiodaa8aabeaak8qacaWGdbGaam4taiaad+eaca WGibGaey4kaSIaamOtaiaadggapaWaaSbaaSqaa8qacaaIYaaapaqa baGcpeGaam4qaiaad+eapaWaaSbaaSqaa8qacaaIZaaapaqabaGcpe GaeyOKH4QaaGOmaiaaykW7caWGdbGaamisa8aadaWgaaWcbaWdbiaa iodaa8aabeaak8qacaWGdbGaam4taiaad+eacaWGobGaamyyaiabgU caRiaadIeapaWaaSbaaSqaa8qacaaIYaaapaqabaGcpeGaam4taiab gUcaRiaadoeacaWGpbWdamaaBaaaleaapeGaaGOmaaWdaeqaaaaa@5CEE@

Reactions involved in test tube B

Ca ( OH ) 2 +C O 2 CaC O 3 + H 2 O MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaadggapaWaaeWaaeaapeGa am4taiaadIeaa8aacaGLOaGaayzkaaWaaSbaaSqaa8qacaaIYaaapa qabaGcpeGaey4kaSIaam4qaiaad+eapaWaaSbaaSqaa8qacaaIYaaa paqabaGcpeGaeyOKH4Qaam4qaiaadggacaWGdbGaam4ta8aadaWgaa WcbaWdbiaaiodaa8aabeaak8qacqGHRaWkcaWGibWdamaaBaaaleaa peGaaGOmaaWdaeqaaOWdbiaad+eaaaa@4F92@

(c) Ethanol ( C 2 H 5 OH MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGynaaWdaeqaaOWdbi aad+eacaWGibaaaa@413B@  ) does not react with sodium carbonate ( N a 2 C O 3 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaamOtaiaadggapaWaaSbaaSqaa8qa caaIYaaapaqabaGcpeGaam4qaiaad+eapaWaaSbaaSqaa8qacaaIZa aapaqabaaaaa@413E@  ). Hence, a similar change is not expected.

C 2 H 5 OH+N a 2 C O 3 No change MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGynaaWdaeqaaOWdbi aad+eacaWGibGaey4kaSIaamOtaiaadggapaWaaSbaaSqaa8qacaaI YaaapaqabaGcpeGaam4qaiaad+eapaWaaSbaaSqaa8qacaaIZaaapa qabaGcpeGaeyOKH4QaamOtaiaad+gacaqGGaGaam4yaiaadIgacaWG HbGaamOBaiaadEgacaWGLbaaaa@51AE@

(d)   When calcium oxide is dissolved in water and the supernatant liquid is decanted, lime water is obtained.

Question: 54

How would you bring about the following conversions?

Name the process and write the reaction involved.

(a) Ethanol to ethene.

(b) Propanol to propanoic acid.

Solution:

(a)   By the dehydration of ethanol in the presence of concentrated H 2 S O 4 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaamisa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGtbGaam4ta8aadaWgaaWcbaWdbiaaisdaa8aabe aaaaa@4063@ ,

C 2 H 5 OH 443K Hotconc. H 2 S O 4 C H 2 =C H 2 + H 2 O MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garuatP5wD4bctPjwzYrxAUvgarmWu51MyVXgaruWq VvNCPvMCG4uz3bqefqvATv2CG4uz3bIuV1wyUbqee0evGueE0jxyai baieYlh91rFfeu0dXdh9vqqj=hEeeu0xXdbba9frFj0=OqFfea0dXd d9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr0=vqpW qaaiaacaWaamaadaGabiaaeaqbayaaaOqaaiaadoeadaWgaaWcbaGa aGOmaaqabaGccaWGibWaaSbaaSqaaiaaiwdaaeqaaOGaam4taiaadI eacaaMc8+aa4alaSqaaiaadIeacaWGVbGaamiDaiaaykW7caWGJbGa am4Baiaad6gacaWGJbGaaGPaVlaac6cacaaMc8UaamisamaaBaaame aacaaIYaaabeaaliaadofacaWGpbWaaSbaaWqaaiaaisdaaeqaaaWc baGaaGinaiaaisdacaaIZaGaaGPaVlaaykW7caWGlbaakiaawkziai aaykW7caaMc8Uaam4qaiaadIeadaWgaaWcbaGaaGOmaaqabaGccqGH 9aqpcaWGdbGaamisamaaBaaaleaacaaIYaaabeaakiabgUcaRiaadI eadaWgaaWcbaGaaGOmaaqabaGccaWGpbaaaa@6C9A@

(b)   By the oxidation of propanol using oxidizing agent such as alkaline KMn O 4 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4saiaad2eacaWGUbGaam4ta8aa daWgaaWcbaWdbiaaisdaa8aabeaaaaa@4023@ ,

C H 3 C H 2 C H 2 OH Heat AIk.KMnO C H 3 C H 2 COOH MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garuatP5wD4bctPjwzYrxAUvgarmWu51MyVXgaruWq VvNCPvMCG4uz3bqefqvATv2CG4uz3bIuV1wyUbqee0evGueE0jxyai baieYlh91rFfeu0dXdh9vqqj=hEeeu0xXdbba9frFj0=OqFfea0dXd d9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr0=vqpW qaaiaacaWaamaadaGabiaaeaqbayaaaOqaaiaadoeacaWGibWaaSba aSqaaiaaiodaaeqaaOGaam4qaiaadIeadaWgaaWcbaGaaGOmaaqaba GccaWGdbGaamisamaaBaaaleaacaaIYaaabeaakiaad+eacaWGibGa aGPaVpaaoWcaleaacaWGbbGaamysaiaadUgacaaMc8UaaiOlaiaayk W7caWGlbGaamytaiaad6gacaWGpbaabaGaamisaiaadwgacaWGHbGa amiDaaGccaGLsgcacaaMc8UaaGPaVlaadoeacaWGibWaaSbaaSqaai aaiodaaeqaaOGaam4qaiaadIeadaWgaaWcbaGaaGOmaaqabaGccaWG dbGaam4taiaad+eacaWGibaaaa@667C@

Question: 55

Draw the possible isomers of the compound with molecular formula C 3 H 6 O MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaioda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGOnaaWdaeqaaOWdbi aad+eaaaa@4070@  and also give their electron dot structures.

Solution:

Question: 56

Explain the given reactions with the examples:

(a) Hydrogenation reaction

(b) Oxidation reaction

(c) Substitution reaction

(d) Saponification reaction

(e) Combustion reaction

Solution:

(a)   Hydrogenation reaction :

The addition of hydrogen to an unsaturated hydrocarbon to make it saturated is known as hydrogenation reaction.

Example:

Vegetable oil ( Unsaturated fat )+Hydrogen MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaamOvaiaadwgacaWGNbGaamyzaiaa dshacaWGHbGaamOyaiaadYgacaWGLbGaaeiiaiaad+gacaWGPbGaam iBaiaabccapaWaaeWaaeaapeGaamyvaiaad6gacaWGZbGaamyyaiaa dshacaWG1bGaamOCaiaadggacaWG0bGaamyzaiaadsgacaqGGaGaam OzaiaadggacaWG0baapaGaayjkaiaawMcaa8qacqGHRaWkcaWGibGa amyEaiaadsgacaWGYbGaam4BaiaadEgacaWGLbGaamOBaaaa@5FBC@  

Vegetable ghee (Saturated fat) MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaaGPaVlaaykW7caaMc8UaaGPaVlaa ykW7caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaG PaVlaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaeyOKH4QaamOvaiaa dwgacaWGNbGaamyzaiaadshacaWGHbGaamOyaiaadYgacaWGLbGaae iiaiaadEgacaWGObGaamyzaiaadwgacaqGGaWdaiaacIcapeGaam4u aiaadggacaWG0bGaamyDaiaadkhacaWGHbGaamiDaiaadwgacaWGKb GaaiiOaiaaykW7caWGMbGaamyyaiaadshapaGaaiykaaaa@75DE@

(b)   Oxidation reaction: The reaction which involves addition of oxygen to a reactant or removal of hydrogen from a reactant is called oxidation reaction.

Example:  Methane reacts with oxygen to form carbon dioxide and water. Here methane is oxidised to carbon dioxide.

(c)    Substitution reaction: When an atom or a group of atoms substitutes another atom or a group of atoms from the molecule, it is known as substitution reaction.

Example: In the presence of sunlight, chlorine is added to methane to form methyl chloride and hydrochloric acid.

C H 4 +C l 2 C H 3 Cl+HCl MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaadIeapaWaaSbaaSqaa8qa caaI0aaapaqabaGcpeGaey4kaSIaam4qaiaadYgapaWaaSbaaSqaa8 qacaaIYaaapaqabaGcpeGaeyOKH4Qaam4qaiaadIeapaWaaSbaaSqa a8qacaaIZaaapaqabaGcpeGaam4qaiaadYgacqGHRaWkcaWGibGaam 4qaiaadYgaaaa@4C08@

(d)   Saponification: A reaction in which an ester is hydrolysed in the presence of a base is called saponification reaction.

Example: It is used in the preparation of soap.

C H 3 COO C 2 H 5 +NaOH C H 3 COONa+ C 2 H 5 OH MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaadIeapaWaaSbaaSqaa8qa caaIZaaapaqabaGcpeGaam4qaiaad+eacaWGpbGaam4qa8aadaWgaa WcbaWdbiaaikdaa8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGyn aaWdaeqaaOWdbiabgUcaRiaad6eacaWGHbGaam4taiaadIeacaqGGa GaeyOKH4Qaam4qaiaadIeapaWaaSbaaSqaa8qacaaIZaaapaqabaGc peGaam4qaiaad+eacaWGpbGaamOtaiaadggacqGHRaWkcaWGdbWdam aaBaaaleaapeGaaGOmaaWdaeqaaOWdbiaadIeapaWaaSbaaSqaa8qa caaI1aaapaqabaGcpeGaam4taiaadIeaaaa@5906@

(e) Combustion reaction: A reaction, in which organic compounds burn readily in air to form CO2 and water vapour along with lot of heat, is known as combustion reaction.

Example: Methane burns in air to form carbon dioxide and water, releasing large amount of heat and light.

C H 4 +2 O 2 C O 2 +2 H 2 O+Heat and light MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaadIeapaWaaSbaaSqaa8qa caaI0aaapaqabaGcpeGaey4kaSIaaGOmaiaaykW7caWGpbWdamaaBa aaleaapeGaaGOmaaWdaeqaaOWdbiabgkziUkaadoeacaWGpbWdamaa BaaaleaapeGaaGOmaaWdaeqaaOWdbiabgUcaRiaaikdacaaMc8Uaam isa8aadaWgaaWcbaWdbiaaikdaa8aabeaak8qacaWGpbGaey4kaSIa amisaiaadwgacaWGHbGaamiDaiaabccacaWGHbGaamOBaiaadsgaca qGGaGaamiBaiaadMgacaWGNbGaamiAaiaadshaaaa@5B7A@

Question: 57

An organic compound A on heating with concentrated H 2 S O 4 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaamisa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGtbGaam4ta8aadaWgaaWcbaWdbiaaisdaa8aabe aaaaa@4063@  forms a compound B which on addition of one mole of hydrogen in the presence of Ni forms a compound C. One mole of compound C on combustion forms two moles of C O 2 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaad+eapaWaaSbaaSqaa8qa caaIYaaapaqabaaaaa@3E54@  and 3 moles of H 2 O MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaamisa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGpbaaaa@3E73@ . Identify the compounds A, B and C and write the chemical equations of the reactions involved.

Solution:

One mole of compound C on combustion forms two moles of C O 2 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qaiaad+eapaWaaSbaaSqaa8qa caaIYaaapaqabaaaaa@3E54@  and 3 moles of H 2 O MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaamisa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGpbaaaa@3E73@ . This means that the compound has at least 2 carbon atoms and 6 hydrogen atoms. Thus, the molecular formula of C is C 2 H 6 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGOnaaWdaeqaaaaa@3F81@  (ethane).

Compound C, i.e. ethane, is obtained by the addition of one mole of hydrogen ( H 2 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaamisa8aadaWgaaWcbaWdbiaaikda a8aabeaaaaa@3D85@  ) to compound B. Thus, compound B should be C 2 H 4 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGinaaWdaeqaaaaa@3F7F@  (ethene).

Compound B, i.e. ethene, is obtained by heating the compound A with concentrated H 2 S O 4 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaamisa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGtbGaam4ta8aadaWgaaWcbaWdbiaaisdaa8aabe aaaaa@4063@  which shows it to be an alcohol. So compound A could be C 2 H 5 OH MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGynaaWdaeqaaOWdbi aad+eacaWGibaaaa@413B@  (ethanol).

C H 3 C H 2 OH Hot Conc. H 2 S O 4 C 2 H 4 +  H 2 O A        B C 2 H 4 + H 2 Ni C 2 H 6 B        C 2 C 2 H 6 +7 O 2 4C O 2 +6 H 2 O+Heat and light C MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garuatP5wD4bctPjwzYrxAUvgarmWu51MyVXgaruWq VvNCPvMCG4uz3bqefqvATv2CG4uz3bIuV1wyUbqee0evGueE0jxyai baieYlh91rFfeu0dXdh9vqqj=hEeeu0xXdbba9frFj0=OqFfea0dXd d9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr0=vqpW qaaiaacaWaamaadaGabiaaeaqbayaaaOabaeqabaaeaaaaaaaaa8qa caWGdbGaamisa8aadaWgaaWcbaWdbiaaiodaa8aabeaak8qacaWGdb Gaamisa8aadaWgaaWcbaWdbiaaikdaa8aabeaak8qacaWGpbGaamis amaaoqcaleaaiiGacaWFibGaa83Baiaa=rhacaWFGaGaa83qaiaa=9 gacaWFUbGaa83yaiaa=5cacaWFGaGaa8hsa8aadaWgaaadbaWdbiaa ikdaa8aabeaal8qacaWFtbGaa83ta8aadaWgaaadbaWdbiaaisdaa8 aabeaaaSWdbeqakiaawkziaiaaykW7caaMc8Uaam4qa8aadaWgaaWc baWdbiaaikdaa8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGinaa WdaeqaaOWdbiabgUcaRiaabccacaWGibWdamaaBaaaleaapeGaaGOm aaWdaeqaaOWdbiaad+eaaeabadWdaiaaykW7caaMc8UaaGPaVlaayk W7caaMc8UaaGPaVlaadgeapeGaaiiOaiaacckacaGGGcGaaiiOaiaa cckacaGGGcGaaiiOaiaacckacaaMc8UaaGPaVlaaykW7caaMc8UaaG PaVlaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7caaM c8UaaGPaVlaaykW7paGaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7ca aMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaa ykW7caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaG PaVlaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7caaM c8UaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaayk W7caWGcbaabqaWa8qacaWGdbWdamaaBaaaleaapeGaaGOmaaWdaeqa aOWdbiaadIeapaWaaSbaaSqaa8qacaaI0aaapaqabaGcpeGaey4kaS Iaamisa8aadaWgaaWcbaWdbiaaikdaa8aabeaak8qadaGdKaWcbaGa amOtaiaadMgaaeqakiaawkziaiaaykW7caaMc8Uaam4qa8aadaWgaa WcbaWdbiaaikdaa8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGOn aaWdaeqaaaGcpeqaeamapaGaaGPaVlaaykW7caaMc8UaaGPaVlaayk W7caWGcbWdbiaacckacaGGGcGaaiiOaiaacckacaGGGcGaaiiOaiaa cckacaGGGcGaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaG PaVlaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7caaM c8+daiaaykW7caaMc8UaaGPaVlaaykW7caaMc8UaaGPaVlaaykW7ca aMc8UaaGPaVlaaykW7caaMc8Uaam4qaaqaeamapeGaaGOmaiaaykW7 caWGdbWdamaaBaaaleaapeGaaGOmaaWdaeqaaOWdbiaadIeapaWaaS baaSqaa8qacaaI2aaapaqabaGcpeGaey4kaSIaaG4naiaaykW7caWG pbWdamaaBaaaleaapeGaaGOmaaWdaeqaaOWdbiabgkziUkaaisdaca aMc8Uaam4qaiaad+eapaWaaSbaaSqaa8qacaaIYaaapaqabaGcpeGa ey4kaSIaaGOnaiaaykW7caWGibWdamaaBaaaleaapeGaaGOmaaWdae qaaOWdbiaad+eacqGHRaWkcaWGibGaamyzaiaadggacaWG0bGaaeii aiaadggacaWGUbGaamizaiaabccacaWGSbGaamyAaiaadEgacaWGOb GaamiDaaqaeamacaaMc8UaaGPaVlaaykW7caaMc8Uaam4qaaaaaa@4524@  

A is ethanol ( C 2 H 5 OH MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGynaaWdaeqaaOWdbi aad+eacaWGibaaaa@413B@  )

B is ethene ( C 2 H 4 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGinaaWdaeqaaaaa@3F7F@  )

C is ethane ( C 2 H 6 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbmLMB1H hicL2BSLMB11garmWu51MyVXgaruWqVvNCPvMCG4uz3bqefqvATv2C G4uz3bIuV1wyUbqee0evGueE0jxyaibaieYlh91rFfeu0dXdh9vqqj =hEeeu0xXdbba9frFj0=OqFfea0dXdd9vqaq=JfrVkFHe9pgea0dXd ar=Jb9hs0dXdbPYxe9vr0=vr0=vqpWqaaeaabaGaciaacaqabeaada abauaaaOqaaabaaaaaaaaapeGaam4qa8aadaWgaaWcbaWdbiaaikda a8aabeaak8qacaWGibWdamaaBaaaleaapeGaaGOnaaWdaeqaaaaa@3F81@  )