CARBOXYLIC ACIDS
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28460 Which of the following carboxylic acids is difficult to decarboxylate

1 828-a807
2 828-b807
3 828-c807
4 828-d807
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28461 In the reaction \(R - X\xrightarrow[{alcoholic}]{{KCN}}A\xrightarrow[\Delta ]{{{H_2}O/{H^ \oplus }}}B,\) product \((B)\) is

1 Alkyl chloride
2 Aldehyde
3 Carboxylic acid
4 Ketone
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28462 Starting from propanoic acid the following reactions were carried out as following \(CH_3 - CH_2 - COOH\) \(\xrightarrow{{SOC{l_2}}}\left[ X \right]\xrightarrow[\Delta ]{{N{H_3}}}\left[ Y \right]\xrightarrow[{KOH}]{{B{r_2}}}\left[ Z \right]\) Product \([Z]\) will be?

1 \(CH_3-CH_2-Br\)
2 \(CH_3-CH_2-NH_2\)
3 \(CH_3-CH_2-COBr\)
4 \(CH_3-CH_2-CH_2-NH_2\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28463 \(C\) is ?

1 818-a1075
2 818-b1075
3 818-c1075
4 818-d1075
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28460 Which of the following carboxylic acids is difficult to decarboxylate

1 828-a807
2 828-b807
3 828-c807
4 828-d807
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28461 In the reaction \(R - X\xrightarrow[{alcoholic}]{{KCN}}A\xrightarrow[\Delta ]{{{H_2}O/{H^ \oplus }}}B,\) product \((B)\) is

1 Alkyl chloride
2 Aldehyde
3 Carboxylic acid
4 Ketone
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28462 Starting from propanoic acid the following reactions were carried out as following \(CH_3 - CH_2 - COOH\) \(\xrightarrow{{SOC{l_2}}}\left[ X \right]\xrightarrow[\Delta ]{{N{H_3}}}\left[ Y \right]\xrightarrow[{KOH}]{{B{r_2}}}\left[ Z \right]\) Product \([Z]\) will be?

1 \(CH_3-CH_2-Br\)
2 \(CH_3-CH_2-NH_2\)
3 \(CH_3-CH_2-COBr\)
4 \(CH_3-CH_2-CH_2-NH_2\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28463 \(C\) is ?

1 818-a1075
2 818-b1075
3 818-c1075
4 818-d1075
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28460 Which of the following carboxylic acids is difficult to decarboxylate

1 828-a807
2 828-b807
3 828-c807
4 828-d807
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28461 In the reaction \(R - X\xrightarrow[{alcoholic}]{{KCN}}A\xrightarrow[\Delta ]{{{H_2}O/{H^ \oplus }}}B,\) product \((B)\) is

1 Alkyl chloride
2 Aldehyde
3 Carboxylic acid
4 Ketone
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28462 Starting from propanoic acid the following reactions were carried out as following \(CH_3 - CH_2 - COOH\) \(\xrightarrow{{SOC{l_2}}}\left[ X \right]\xrightarrow[\Delta ]{{N{H_3}}}\left[ Y \right]\xrightarrow[{KOH}]{{B{r_2}}}\left[ Z \right]\) Product \([Z]\) will be?

1 \(CH_3-CH_2-Br\)
2 \(CH_3-CH_2-NH_2\)
3 \(CH_3-CH_2-COBr\)
4 \(CH_3-CH_2-CH_2-NH_2\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28463 \(C\) is ?

1 818-a1075
2 818-b1075
3 818-c1075
4 818-d1075
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28460 Which of the following carboxylic acids is difficult to decarboxylate

1 828-a807
2 828-b807
3 828-c807
4 828-d807
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28461 In the reaction \(R - X\xrightarrow[{alcoholic}]{{KCN}}A\xrightarrow[\Delta ]{{{H_2}O/{H^ \oplus }}}B,\) product \((B)\) is

1 Alkyl chloride
2 Aldehyde
3 Carboxylic acid
4 Ketone
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28462 Starting from propanoic acid the following reactions were carried out as following \(CH_3 - CH_2 - COOH\) \(\xrightarrow{{SOC{l_2}}}\left[ X \right]\xrightarrow[\Delta ]{{N{H_3}}}\left[ Y \right]\xrightarrow[{KOH}]{{B{r_2}}}\left[ Z \right]\) Product \([Z]\) will be?

1 \(CH_3-CH_2-Br\)
2 \(CH_3-CH_2-NH_2\)
3 \(CH_3-CH_2-COBr\)
4 \(CH_3-CH_2-CH_2-NH_2\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28463 \(C\) is ?

1 818-a1075
2 818-b1075
3 818-c1075
4 818-d1075