Product of the Wolff-Kishner reduction is-

Important Questions on Aldehydes, Ketones and Carboxylic Acids

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Alpha Question Bank for Medical: Chemistry>Chapter 25 - Aldehydes, Ketones and Carboxylic Acids>Exercise 2>Q 70

Wolff-Kishner reduction cannot be used in which of the following:

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Alpha Question Bank for Medical: Chemistry>Chapter 25 - Aldehydes, Ketones and Carboxylic Acids>Exercise 2>Q 71

Clemmensen reduction cannot be used in which of the following?

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Alpha Question Bank for Medical: Chemistry>Chapter 25 - Aldehydes, Ketones and Carboxylic Acids>Exercise 2>Q 72

An unknown compound decolorizes bromine in carbon tetrachloride, and it undergoes catalytic reduction to give decalin. When treated with warm, conc. potassium permangate, this compound give ciscyclohexane-$1,2$-dicaboxylic acid and oxalic acid. Possible structure for the unknown compound is-

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Alpha Question Bank for Medical: Chemistry>Chapter 25 - Aldehydes, Ketones and Carboxylic Acids>Exercise 2>Q 73

In the reaction,

${\mathrm{CH}}_3\mathrm{COOH}\stackrel{{\mathrm{LiAlH}}_4}{\to }\mathrm{A}\stackrel{{\mathrm{PCl}}_5}{\to }\mathrm{B}\stackrel{{\mathrm{NaNH}}_2,\mathrm{\Delta }}{\to }\mathrm{C}$,

$\mathrm{C}$ is  -

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Alpha Question Bank for Medical: Chemistry>Chapter 25 - Aldehydes, Ketones and Carboxylic Acids>Exercise 2>Q 74

....is obtained when iodoform is heated with $\mathrm{Ag}$ powder:

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Alpha Question Bank for Medical: Chemistry>Chapter 25 - Aldehydes, Ketones and Carboxylic Acids>Exercise 2>Q 75

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Alpha Question Bank for Medical: Chemistry>Chapter 25 - Aldehydes, Ketones and Carboxylic Acids>Exercise 2>Q 76

$\left(\mathrm{X}\right) \left({\mathrm{C}}_6{\mathrm{H}}_3\mathrm{CIBrCOOH}\right)$ are dihalosubstituted benzoic acids. The strongest acid among all isomers is:

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Alpha Question Bank for Medical: Chemistry>Chapter 25 - Aldehydes, Ketones and Carboxylic Acids>Exercise 2>Q 77