Acid Derivatives
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323402 Among the given compounds, the most susceptible to nucleophilic attack at the carbonyl group is

1 \(\mathrm{MeCOCl}\)
2 \(\mathrm{MeCHO}\)
3 \(\mathrm{MeCOOMe}\)
4 \(\mathrm{MeCOOCOMe}\)
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323403 Acids can be prepared by the hydrolysis of

1 cyanides
2 amides
3 esters
4 all of these.
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323404 Benzamide on reaction with \(\mathrm{POCl}_{3}\) gives

1 Aniline
2 Chlorobenzene
3 Benzyl amine
4 Benzonitrile
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323405 The main product obtained in the reaction of acetamide and \(\mathrm{HNO}_{2}\) is

1 \(\mathrm{CH}_{3} \mathrm{CN}\)
2 \(\mathrm{CH}_{3} \mathrm{NC}\)
3 \(\mathrm{CH}_{3} \mathrm{NH}_{2}\)
4 \(\mathrm{CH}_{3} \mathrm{COOH}\)
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323402 Among the given compounds, the most susceptible to nucleophilic attack at the carbonyl group is

1 \(\mathrm{MeCOCl}\)
2 \(\mathrm{MeCHO}\)
3 \(\mathrm{MeCOOMe}\)
4 \(\mathrm{MeCOOCOMe}\)
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323403 Acids can be prepared by the hydrolysis of

1 cyanides
2 amides
3 esters
4 all of these.
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323404 Benzamide on reaction with \(\mathrm{POCl}_{3}\) gives

1 Aniline
2 Chlorobenzene
3 Benzyl amine
4 Benzonitrile
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323405 The main product obtained in the reaction of acetamide and \(\mathrm{HNO}_{2}\) is

1 \(\mathrm{CH}_{3} \mathrm{CN}\)
2 \(\mathrm{CH}_{3} \mathrm{NC}\)
3 \(\mathrm{CH}_{3} \mathrm{NH}_{2}\)
4 \(\mathrm{CH}_{3} \mathrm{COOH}\)
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323402 Among the given compounds, the most susceptible to nucleophilic attack at the carbonyl group is

1 \(\mathrm{MeCOCl}\)
2 \(\mathrm{MeCHO}\)
3 \(\mathrm{MeCOOMe}\)
4 \(\mathrm{MeCOOCOMe}\)
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323403 Acids can be prepared by the hydrolysis of

1 cyanides
2 amides
3 esters
4 all of these.
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323404 Benzamide on reaction with \(\mathrm{POCl}_{3}\) gives

1 Aniline
2 Chlorobenzene
3 Benzyl amine
4 Benzonitrile
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323405 The main product obtained in the reaction of acetamide and \(\mathrm{HNO}_{2}\) is

1 \(\mathrm{CH}_{3} \mathrm{CN}\)
2 \(\mathrm{CH}_{3} \mathrm{NC}\)
3 \(\mathrm{CH}_{3} \mathrm{NH}_{2}\)
4 \(\mathrm{CH}_{3} \mathrm{COOH}\)
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323402 Among the given compounds, the most susceptible to nucleophilic attack at the carbonyl group is

1 \(\mathrm{MeCOCl}\)
2 \(\mathrm{MeCHO}\)
3 \(\mathrm{MeCOOMe}\)
4 \(\mathrm{MeCOOCOMe}\)
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323403 Acids can be prepared by the hydrolysis of

1 cyanides
2 amides
3 esters
4 all of these.
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323404 Benzamide on reaction with \(\mathrm{POCl}_{3}\) gives

1 Aniline
2 Chlorobenzene
3 Benzyl amine
4 Benzonitrile
CHXII12:ALDEHYDES KETONES AND CARBOXYLIC ACIDS

323405 The main product obtained in the reaction of acetamide and \(\mathrm{HNO}_{2}\) is

1 \(\mathrm{CH}_{3} \mathrm{CN}\)
2 \(\mathrm{CH}_{3} \mathrm{NC}\)
3 \(\mathrm{CH}_{3} \mathrm{NH}_{2}\)
4 \(\mathrm{CH}_{3} \mathrm{COOH}\)