Important Questions of Aldehydes, Ketones and Carboxylic Acids Chemistry | Zigya

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 Multiple Choice QuestionsMultiple Choice Questions

1111.

The Kolbe's electrolysis proceeds via

  • nucleophilic substitution mechanism

  • electrophilic addition mechanism

  • free radical mechanism

  • electrophilic substitution reaction


1112.

Benedict's solution is not reduced by :

  • formaldehyde

  • acetaldehyde

  • glucose

  • acetic anhydride


1113.

The reagent used in Gatterman Koch aldehyde synthesis is :-

  • Pb/ BaSO4

  • alkaline KMnO4

  • acidic KMnO4

  • CO + HCl


1114.

Iodoform can be obtained on warming NaOH and iodine with

  • CH3-CH2-CH(OH)CH3

  • (CH3)2CH-CO-C2H5

  • CH3-CO-OCH3

  • (CH3)3CCH2OH


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1115.

Aldol condensation will not occur in :

  • HCHO

  • CH3CH2CHO

  • CH3COCH3

  • CH3CHO


1116.

Ethers are isomeric with

  • aldehyde

  • ketones

  • both aldehyde and ketones

  • alcohols


1117.

In Williamson's synthesis

  • an alkyl halide is treated with sodium alkoxide

  • an alkyl halide is treated with sodium

  • an alcohol is heated with cone. H2SO4  at 130°C

  • None of the above


1118.

The Cannizaro reaction is not given by

  • trimethyl acetaldehyde

  • acetaldehyde

  • benzaldehyde

  • formaldehyde


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1119.

Self condensation of acetaldehyde, in the presence of dilute alkalies gives

  • an acetal

  • an aldol

  • mesitylene

  • propionaldehyde


1120.

Stephen's reduction is used to prepare aldehyde from

  • alcohol

  • alkyl cyanides

  • alkanones

  • acid chlorides


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