The correct sequence of reactions to be performed to convert benz

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 Multiple Choice QuestionsMultiple Choice Questions

441.

Which one of these is not true for benzene?

  • It forms only one type of monosubstituted product

  • There are three carbon-carbon single bonds and three carbon-carbon double bonds

  • Heat of hydrogenation of benzene is less than its theoretical value

  • The bond angle between carbon-carbon bonds is 120°


442.

A dibromo derivative of an alkane reacts with sodium metal to form an alicyclic hydrocarbon. The derivative is

  • 1, 1-dibromopropane

  • 2, 2-dibromobutane

  • 1, 2-dibromoethane

  • 1, 4-dibromobutane


443.

Which one of the following is an intermediate in the reaction of benzene with CH3Cl in the presence of anhydrous AlCl3?

  • Cl-

  • CH3-

  • CH3+


444.

Cycloalkane formed when 1,4-dibromopentaneis heated with sodium is

  • methyl cyclobutane

  • cyclopentane

  • cyclobutane

  • methyl cyclopentane


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445.

Methane can be converted into ethane by the reactions

  • chlorination followed by the reaction with alcoholic KOH

  • chlorination followed by the reaction with aqueous KOH

  • chlorination followed by Wurtz reaction

  • chlorination followed by decarboxylation


446.

Least energetic conformation of cyclohexane is

  • chair conformation

  • boat conformation

  • cis conformation

  • E-Z form


447.

An alkyl bromide (X) reacts with sodium in ether to form 4,5-dIethyl octane, the compound X is

  • CH3(CH2)3Br

  • CH3(CH2)5Br

  • CH3(CH2)3CH(Br)CH3

  • CH3—(CH2)2—CH(Br)—CH2—CH3


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448.

The correct sequence of reactions to be performed to convert benzene into m-bromoaniline is

  • nitration, reduction, bromination

  • bromination, nitration, reduction

  • nitration, bromination, reduction

  • reduction, nitration, bromination


C.

nitration, bromination, reduction

Conversion of benzene into m-bromoaniline can be done by successive nitration, bromination and reduction using following reagent:

     Nitration : conc. HNO3 | conc. H2SO4

Bromination : Br2 | H2O

   Reduction : Sn | HCl

Formation of nitrobenzene in the first step direct incoming electrophile towards meta position on the further step reduction of nitro compound produces m- bromoaniline very easily. Complete sequence of the chemical reaction can be shown as-


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449.

The correct statement is

  • Cyclohexadene and cyclohexene cannot be isolated with ease during controlled hydrogenation of benzene

  • One mole each of benzene and hydrogen when reacted gives 1/3 mole of cyclohexane and 2/3 mole unreacted hydrogen

  • Hydrogenation of benzene to cyclohexane is an endothermic process

  • It is easier to hydrogenate benzene when compared to cyclohexene


450.

Number of possible alkynes with formula C5H8 is

  • 2

  • 3

  • 4

  • 5


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