Name the following halides according to IUPAC system and classify them as alkyl, allyl, and benzyl (primary, secondary, tertiary), and vinyl or aryl halides:

(i) (CH₃)₂CHCH (Cl) CH3

(ii) CH₃CH₂CH (CH₃) CH (C₂H₅) Cl

(iii) CH₃CH₂C (CH₃)₂CH₂I 

(iv) (CH₃)₃CCH₂CH (Br) C6H5

(v) CH₃CH(CH₃)CH(Br)CH₃

(vi) CH₃C(C₂H₅)2CH₂Br

(vii) CH₃C(Cl)(C₂H₅)CH₂CH₃ 

(viii) CH₃CH=C (Cl) CH₂CH (CH₃)₂

(viii) CH₃CH=CHC (Br) (CH₃)₂

(ix) p-ClC₆H₄CH₂CH (CH₃)₂

(x) m-ClCH₂C₆H₄CH₂C (CH₃)₃

(xi) o-Br-C₆H₄CH (CH₃) CH₂CH₃

Give the IUPAC names of the following compounds:

(i) CH₃CH (Cl) CH (Br) CH₃

(ii) CHF₂CBrClF

(iii) ClCH₂C≡CCH₂Br

(iv) (CCl₃)₃CCl

(v) CH₃C (p-ClC₆H₄)2CH (Br) CH₃ 

(vi) (CH₃) 3CCH=ClC₆H₄I-p

Write the structures of the following organic halogen compounds.

(i) 2-Chloro-3-methylpentane

(ii) p-Bromochlorobenzene

(iii) 1-Chloro-4-ethylcyclohexane

(iv) 2-(2-Chlorophenyl)-1-iodooctane

(v) Perfluorobenzene

(vi) 4-tert-Butyl-3-iodoheptane

(vii) 1-Bromo-4-sec-butyl-2-methylbenzene

(viii) 1, 4-Dibromobut-2-ene

Which one of the following has the highest dipole moment?

(i) CH₂Cl₂

(ii) CHCl₃

(iii) CCl₄

A hydrocarbon C₅H₁₀ does not react with chlorine in dark but gives a single monochloro compound C₅H₉Cl in bright sunlight. Identify the hydrocarbon.

Write the isomers of the compound having formula C₄H₉Br.

Write the equations for the preparation of 1-iodobutane from

(i) 1-butanol

(ii) 1-chlorobutane

(iii) but-1-ene.

What are ambident nucleophiles? Explain with an example.

Which compound in each of the following pairs will react faster in S_N2 reaction with –OH?

(i) CH₃Br or CH₃I

(ii) (CH₃)₃CCl or CH₃Cl.

Predict all the alkenes that would be formed by dehydrohalogenation of the following halides with sodium ethoxide in ethanol and identify the major alkene:

(i) 1-Bromo-1-methylcyclohexane 

(ii) 2-Chloro-2-methylbutane

(iii) 2,2,3-Trimethyl-3-bromopentane

How will you bring about the following conversions?

(i) Ethanol to but-1-yne

(ii) Ethane to bromoethene

(iii) Propene to1nitropropane

(iv) Toluene to benzyl alcohol

(v) Propene to propyne

(vi) Ethanol to ethyl fluoride

(vii) Bromomethane to propanone

(viii) But-1-ene to but-2-ene

(ix) 1-Chlorobutane to n-octane (x) Benzene to biphenyl.

Explain why

(i) The dipole moment of chlorobenzene is lower than that of cyclohexylchloride?

(ii) Alkyl halides, though polar, are immiscible with water?

(iii) Grignard reagents should be prepared under anhydrous conditions?

Give the uses of Freon 12, DDT, carbon tetrachloride and Iodoform.

 

 

 

Write the mechanism of the following reaction:-

 

Arrange the compounds of each set in order of reactivity towards S_N2 displacement:

(i) 2-Bromo-2-methylbutane, 1-Bromopentane, 2-Bromopentane

(ii) 1-Bromo-3-methylbutane, 2-Bromo-2-methylbutane, 3-Bromo-2-

methylbutane

(iii) 1-Bromobutane, 1-Bromo-2, 2-dimethylpropane, 1-Bromo-2-

methylbutane, 1-Bromo-3-methylbutane

Out of C₆H₅CH₂Cl and C₆H₅CHClC₆H₅, which is more easily hydrolysed by aqueous KOH?

p-Dichlorobenzene has higher melting point and solubility than those of o- and m-isomers. Discuss.

How the following conversions can be carried out?

(i) Propene to propan-1-ol

(ii) Ethanol to but-1-yne

(iii) 1-Bromopropane to 2-bromopropane

(iv) Toluene to benzyl alcohol

(v) Benzene to 4-bromonitrobenzene

(vi) Benzyl alcohol to 2-phenylethanoic acid

(vii) Ethanol to propanenitrile

(viii) Aniline to chlorobenzene

(ix) 2-Chlorobutane to 3, 4-dimethylhexane

(x) 2-Methyl-1-propene to 2-chloro-2-methylpropane

(xi) Ethyl chloride to propanoic acid

(xii) But-1-ene to n-butyliodide

(xiii) 2-Chloropropane to 1-propanol

(xiv) Isopropyl alcohol to Iodoform

(xv) Chlorobenzene to p-nitrophenol

(xvi) 2-Bromopropane to 1-bromopropane

(xvii) Chloroethane to butane

(xviii) Benzene to diphenyl

(xxi) tert-Butyl bromide to isobutyl bromide

(xx) Aniline to phenylisocyanide.

The treatment of alkyl chlorides with aqueous KOH leads to the formation of alcohols but in the presence of alcoholic KOH, alkenes are major products.

Explain.

Primary alkyl halide C₄H₉Br

(a) reacted with alcoholic KOH to give compound

(b) is reacted with HBr to give

(c) which is an isomer of (a).

When (a) is reacted with sodium metal it gives compound

(d), C₈H₁₈ which is different from the compound formed when n-butyl bromide is reacted with sodium.

Give the structural formula of (a) and write the equations for all the reactions?

What happens when:- 

(i) n-butyl chloride is treated with alcoholic KOH,

(ii) Bromobenzene is treated with Mg in the presence of dry ether,

(iii) Chlorobenzene is subjected to hydrolysis,

(iv) Ethyl chloride is treated with aqueous KOH,

(v) Methyl bromide is treated with sodium in the presence of dry ether,

(vi) Methyl chloride is treated with KCN??