Hofmann bromamide degradation of amides

1. A.
   $32\text{ }g{\text{ }mol}^{- 1}$
2. B.
   $14\text{ }g{\text{ }mol}^{- 1}$
3. C.
   $28\text{ }g{\text{ }mol}^{- 1}$
4. D.
   $30\text{ }g{\text{ }mol}^{- 1}$

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1. A.
   ${CH}_{4}$
2. B.
   ${CH}_{3}COOH$
3. C.
   $\ {CH}_{3}{CH}_{2}{NH}_{2}$
4. D.
   $\ {CH}_{3}{NH}_{2}$

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1. A.
   It is useful to convert amides to primary amines.
2. B.
   In this -CO-group is reduced to $\mathrm{-CH_2-}$ group.
3. C.
   Molar mass of the amine obtained is always less than the amide.
4. D.
   The reagent used is $\mathrm{Br_2}$ and $\mathrm{KOH_{(aq)}}$ .

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1. A.
   $\mathrm{CH_3CH_2CH_2COOH}$
2. B.
   $\mathrm{CH_3COCH_3}$
3. C.
   $\mathrm{CH_3CH_2NH_2}$
4. D.
   $\mathrm{CH_3CH_2Br}$

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1. A.
   Gabriel phthalimide synthesis
2. B.
   Ammonolysis of halides
3. C.
   Mendius reduction
4. D.
   Hofmann degradation

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1. A.
   Gabriel phthalimide reaction
2. B.
   Hofmann elimination reaction
3. C.
   Hofmann exhaustive alkylation reaction
4. D.
   Hofmann degradation reaction

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1. A.
   Friedel-Craft's reaction
2. B.
   Hofmann reaction
3. C.
   Hoffmann bromamide degradation reaction
4. D.
   Hinsberg reaction

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