Chemistry

Hydrocarbons

Question:

Suggest a route for the preparation of nitrobenzene starting from acetylene.

Answer:

Acetylene when passed through red hot iron tube at 500 °C undergoes cyclic polymerisation to give benzene which upon nitration gives nitrobenzene.

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Hydrocarbons

Q 1.

In the alkane, CH3CH2—C(CH3)2—CH2—CH(CH3)2, identify 1 °, 2 °, 3 ° carbon atoms and give the number of H-atoms bonded to each one of these.

Q 2.

Convert ethylene to ethane.

Q 3.

What is the hybridisation of central carbon in 1,2-propadiene (CH2=C=CH2)?

Q 4.

Out of benzene, m-dinitrobenzene and toluene which will undergo nitration most easily and why?

Q 5.

How will you distinguish between propene and propane?

Q 6.

Nucleophiles and electrophiles are reaction intermediates having electron rich and electron deficient centres respectively. Hence, they tend to attack electron deficient and electron rich centres respectively. Classify the following species as electrophiles and nucleophiles.
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Q 7.

What happens when ethanol is heated with cone. H2SO4?

Q 8.

Which of the following are correct?
(a) CH3 – O – CH+2 is more stable than CH3 – CH+2
(b) (CH3)2CH+ is less stable than CH3 – CH2 – CH+2
(c) CH2 = CH – CH+2 is more stable than CH3 – CH2 – CH+2
(d) CH2 = CH+ is more stable than CH3 – CH+2
 

Q 9.

What are conformations?

Q 10.

Write the IUPAC names of the following compounds.
(i) (CH3)CCH2C(CH3)3    (ii) (CH3)2C(C2H5)2

Q 11.

The relative reactivity of 1 °, 2 ° and 3 ° hydrogens towards chlorination is 1: 3.8 : 5. Calculate the percentages of all monochlorinated products obtained from 2-methylbutane.
 

Q 12.

For the following compounds, write structural formulas and IUPAC names for all possible isomers having the number of double or triple bond as indicated:
(a) C4H8 (one double bond) (b) C5H8 (one triple bond)

Q 13.

Arrange the following: HCl, HBr, HI, HF in order of decreasing reactivity towards alkenes.

Q 14.

What happens when benzene is treated with acetyl chloride in presence of AlCl3?

Q 15.

The molecules having dipole moment are________ .
(a) 2,2-Dimethylpropane                                            
(b) trans-Pent-2-ene
(c) cw-Hex-3-ene            
(d) 2,2,3,3-Tetramethylbutane

Q 16.

Which is more acidic: ethene or ethyne and why?

Q 17.

Why does the presence of a nitro group-make the benzene ring less reactive in comparison to the unsubstituted benzene ring? Explain.

Q 18.

Why is benzene extra-ordinarily stable though it contains three double bonds?

Q 19.

Explain why the following systems are not aromatic?
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Q 20.

What effect does branching of an alkane chain has on its boiling point?

Q 21.

Which of the following alkenes on ozonolysis gives a mixture of ketones only?
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Q 22.

Write chemical equations for the combustion reaction of the following hydrocarbons,  (i) Butane (ii) Pentene (iii) Hexyne (iv) Toluene

Q 23.

What effect does branching of an alkane chain has on its boiling point?

Q 24.

What do you mean by pyrolysis?

Q 25.

Why are alkanes called paraffins?

Q 26.

How will you distinguish between acetylene and ethylene?

Q 27.

What is electrophile in sulphonation?

Q 28.

What are Arenes ?

Q 29.

Explain the following with examples:
(i) Wurtz reaction
(ii) Hydrogenation.

Q 30.

Classify the following compounds into (i) alkanes (ii) alkenes (iii) alkynes (iv) arenes.  (a) C6H6 (b) C4H8 (C) C8H8 (d) C5H8 (e) C6H14

Q 31.

What is polymerization? Give an example.

Q 32.

(a) Why are alkenes called unsaturated hydrocarbons?
(b) How will you test the presence of double bond in an alkene?
(c) Name the products formed when propene is subjected to ozonolysis.

Q 33.

How will you separate propene from propyne?

Q 34.

Arrange the following alkyl halides in decreasing order of the rate of β -elimination reaction with alcoholic KOH.

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Q 35.

Arrange the following set of compounds in the order of their decreasing . relative reactivity with an electrophile. Give reason.

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Q 36.

An alkene ‘A’ contains three C—C, eight C—H, a-bonds, and one C—C n-bond. ‘A’ on ozonolysis gives two moles of an aldehyde of molar mass 44 u. Write the IUPAC name of’A’.

Q 37.

What are the necessary conditions for any system to be aromatic?

Q 38.

Arrange the following set of compounds in order of their decreasing relative reactivity with an electrophile, E+.
(a) Chlorobenzene, 2, 4-dinitrochlorobenzene, p-nitrochlorobenzene
(b) Toluene,p—H3C—C6H4—NO2, p—O2N—C6H4—NO2.

Q 39.

What is decarboxylation ? Give an example.

Q 40.

What happens when benzene is treated with acetyl chloride in presence of AlCl3?

Q 41.

Which type of isomerism is exhibited by but-l-yne and but-2-yne?

Q 42.

Discuss the preparation of alkanes by Wurtz reaction. What is the limitaHon of the reaction?

Q 43.

Write the structure of the alkene which on reductive ozonolysis gives butanone and ethanol.

Q 44.

Which are the correct IUPAC names of the following compound
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(a) 5-(2′,2′-Dimethylpropyl)decane
(b) 4-Butyl-2,2-dimethylnonane
(c) 2,2-Dimethyl-4-pentyloctane
(d) 5-neo-Pentyldecane

Q 45.

Alkynes on reduction with sodium in liquid ammonia form trans alkenes. Will butene formed on the reduction of but-2-yne show geometrical isomerism?

Q 46.

Draw Newman and Sawhorse projections for the eclipsed and staggered conformations of ethane. Which of these conformations is more stable and why? .

Q 47.

What happens when benzene is treated with excess of Cl2 in presence of sunlight? Give chemical reaction.

Q 48.

Although benzene is highly unsaturated it does not undergo addition reactions. Why?

Q 49.

Why are Alkenes called olefins?

Q 50.

What is Huckel rule?