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 Multiple Choice QuestionsMultiple Choice Questions

291.

End product of the following reaction is


292.

Which of the following conformers for ethylene glycol is most stable?


293.

The IUPAC name of the compound CH3CH=CHCCH is is

  • pent-4-yn-2-ene

  • pent-3-en-1-yne

  • pent-2-en-4-yne

  • pent-1-yn-3-ene


294.

Consider the reactions,

(CH3)2CH-CH2Br C2H5OH(CH3)2CH-CH2OC2H5 + HBr(CH3)2CH-CH2Br C2H5O-(CH3)2CH-CH2OC2H5 + Br-

The mechanisms of reactions (i) and (ii) are respectively

  • S1 and SN2

  • SN 1 and SN1

  • SN 2 and SN 2

  • SN 2 and SN1


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295.

CH3CH2Br undergoes Wurtz reaction. We may expect some of the following product

A: CH3CH2CH2CH3

B: CH2=CH2

C: CH3-CH3

Select correct product.

  • Only A

  • A and B

  • A, B and C

  • A and C


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296.

Identify the alkyne in the following sequence of reactions,

Alkyne Lindlar's catalystH2A Ozonolysis B only                                                   Wacker processCH2=CH2

  • H3C-CC-CH3

  •  H3C-CH2-CCH 

  • H2C=CH-CCH 

  • HCC-CH2-CCH


A.

H3C-CC-CH3

In Wacker process, alkene is oxidised into aldehyde.

CH2=CH2 + 12O2 H2OPdCl2·CuCl2 CH3CHO(B)

Since on ozonolysis, only alkenes produce aldehydes, 'A' must be an alkene. To decide the structure of alkene that undergoes ozonolysis, bring the products together in such a way that O atoms are face to face and, replace O by double (=) bond. Thus,


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297.

CH3CH3 + HNO3 675K ?

  • CH3CH2NO2

  • CH3CH2NO2 + CH3NO2

  • 2CH3NO2

  • CH2= CH2


298.

In which of the below reaction do we find α,β-unsaturated carbonyl compounds undergoing a ring closure reaction with conjugated dienes?

  • Perkin reaction

  • Diels-Alder reaction

  • Claisen rearrangement

  • Hofmann reaction


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299.

IUPAC name of the compound

  • 5-methyl-4-iso propyl-6, 6' diethyloctane

  • 3,3-dimethyl, 3-ethyl-5-isopropyl octane

  • 3,3-diethyl-4-methyl-5-(1,1-dimethyl) octane

  • 3,3-diethyl-4-methyl-5-(1'-methylethyl) octane


300.

Consider the following carbocations,

(I) C6H5C+H2                        (II) C6H5CH2C+H2(III) C6H5C+HCH3                (IV) C6H5C+(CH3)2

The correct sequence of the stability of these is

  • II < I < III < IV

  • II < III < I < IV

  • III < I < II < IV

  • IV < III < I < II


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