CARBOXYLIC ACIDS
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ALDEHYDES, KETONES AND CARBOXYLIC ACID

28062 The fatty acid which shows reducing property is

1 Acetic acid
2 Ethanoic Acid
3 Oxalic acid
4 Formic acid
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28063 The reagent that can be used to distinguish between methanoic acid and ethanoic acid is

1 Ammoniacal silver nitrate solution
2 Neutral ferric Chloride solution
3 Sodium carbonate solution
4 Phenolphthalein
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28064 Hydrolysis of an ester gives acid \(A\) and alcohol \(B\). \(A\) reduces Fehling solution and oxidation of \(B\) gives \(A\). The ester is

1 Methyl formate
2 Ethyl formate
3 Methyl acetate
4 Ethyl acetate
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28065 Order of reactivity is

1 \(R - \mathop C\limits^{\mathop {||}\limits^O } - X\;\; > RCON{H_2}\;\; > RCOOCOR\;\; > RCOOR\)
2 \(RCOX\; > RCOOCOR\; > RCOOR\; > RCON{H_2}\)
3 \(RCOOR\; > RCON{H_2}\; > RCOX\; > RCOOCOR\)
4 \(RCOOCOR\; > RCOOR\; > RCOX\; > RCON{H_2}\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28066 Right order of acidic strength is

1 \(C{H_2}ClCOOH > HCOOH > \)\({C_2}{H_5}COOH > C{H_3}COOH\)
2 \(C{H_2}ClCOOH\;\; > HCOOH\;\; > \)\(C{H_3}COOH\;\; > {C_2}{H_5}COOH\)
3 \({C_2}{H_5}COOH\;\; > \;C{H_3}COOH\;\; > \)\(HCOOH\;\; > C{H_2}ClCOOH\)
4 \(HCOOH\;\; > C{H_2}ClCOOH\;\; > \)\(C{H_3}COOH\;\; > {C_2}{H_5}COOH\)
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ALDEHYDES, KETONES AND CARBOXYLIC ACID

28062 The fatty acid which shows reducing property is

1 Acetic acid
2 Ethanoic Acid
3 Oxalic acid
4 Formic acid
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28063 The reagent that can be used to distinguish between methanoic acid and ethanoic acid is

1 Ammoniacal silver nitrate solution
2 Neutral ferric Chloride solution
3 Sodium carbonate solution
4 Phenolphthalein
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28064 Hydrolysis of an ester gives acid \(A\) and alcohol \(B\). \(A\) reduces Fehling solution and oxidation of \(B\) gives \(A\). The ester is

1 Methyl formate
2 Ethyl formate
3 Methyl acetate
4 Ethyl acetate
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28065 Order of reactivity is

1 \(R - \mathop C\limits^{\mathop {||}\limits^O } - X\;\; > RCON{H_2}\;\; > RCOOCOR\;\; > RCOOR\)
2 \(RCOX\; > RCOOCOR\; > RCOOR\; > RCON{H_2}\)
3 \(RCOOR\; > RCON{H_2}\; > RCOX\; > RCOOCOR\)
4 \(RCOOCOR\; > RCOOR\; > RCOX\; > RCON{H_2}\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28066 Right order of acidic strength is

1 \(C{H_2}ClCOOH > HCOOH > \)\({C_2}{H_5}COOH > C{H_3}COOH\)
2 \(C{H_2}ClCOOH\;\; > HCOOH\;\; > \)\(C{H_3}COOH\;\; > {C_2}{H_5}COOH\)
3 \({C_2}{H_5}COOH\;\; > \;C{H_3}COOH\;\; > \)\(HCOOH\;\; > C{H_2}ClCOOH\)
4 \(HCOOH\;\; > C{H_2}ClCOOH\;\; > \)\(C{H_3}COOH\;\; > {C_2}{H_5}COOH\)
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ALDEHYDES, KETONES AND CARBOXYLIC ACID

28062 The fatty acid which shows reducing property is

1 Acetic acid
2 Ethanoic Acid
3 Oxalic acid
4 Formic acid
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28063 The reagent that can be used to distinguish between methanoic acid and ethanoic acid is

1 Ammoniacal silver nitrate solution
2 Neutral ferric Chloride solution
3 Sodium carbonate solution
4 Phenolphthalein
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28064 Hydrolysis of an ester gives acid \(A\) and alcohol \(B\). \(A\) reduces Fehling solution and oxidation of \(B\) gives \(A\). The ester is

1 Methyl formate
2 Ethyl formate
3 Methyl acetate
4 Ethyl acetate
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28065 Order of reactivity is

1 \(R - \mathop C\limits^{\mathop {||}\limits^O } - X\;\; > RCON{H_2}\;\; > RCOOCOR\;\; > RCOOR\)
2 \(RCOX\; > RCOOCOR\; > RCOOR\; > RCON{H_2}\)
3 \(RCOOR\; > RCON{H_2}\; > RCOX\; > RCOOCOR\)
4 \(RCOOCOR\; > RCOOR\; > RCOX\; > RCON{H_2}\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28066 Right order of acidic strength is

1 \(C{H_2}ClCOOH > HCOOH > \)\({C_2}{H_5}COOH > C{H_3}COOH\)
2 \(C{H_2}ClCOOH\;\; > HCOOH\;\; > \)\(C{H_3}COOH\;\; > {C_2}{H_5}COOH\)
3 \({C_2}{H_5}COOH\;\; > \;C{H_3}COOH\;\; > \)\(HCOOH\;\; > C{H_2}ClCOOH\)
4 \(HCOOH\;\; > C{H_2}ClCOOH\;\; > \)\(C{H_3}COOH\;\; > {C_2}{H_5}COOH\)
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ALDEHYDES, KETONES AND CARBOXYLIC ACID

28062 The fatty acid which shows reducing property is

1 Acetic acid
2 Ethanoic Acid
3 Oxalic acid
4 Formic acid
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28063 The reagent that can be used to distinguish between methanoic acid and ethanoic acid is

1 Ammoniacal silver nitrate solution
2 Neutral ferric Chloride solution
3 Sodium carbonate solution
4 Phenolphthalein
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28064 Hydrolysis of an ester gives acid \(A\) and alcohol \(B\). \(A\) reduces Fehling solution and oxidation of \(B\) gives \(A\). The ester is

1 Methyl formate
2 Ethyl formate
3 Methyl acetate
4 Ethyl acetate
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28065 Order of reactivity is

1 \(R - \mathop C\limits^{\mathop {||}\limits^O } - X\;\; > RCON{H_2}\;\; > RCOOCOR\;\; > RCOOR\)
2 \(RCOX\; > RCOOCOR\; > RCOOR\; > RCON{H_2}\)
3 \(RCOOR\; > RCON{H_2}\; > RCOX\; > RCOOCOR\)
4 \(RCOOCOR\; > RCOOR\; > RCOX\; > RCON{H_2}\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28066 Right order of acidic strength is

1 \(C{H_2}ClCOOH > HCOOH > \)\({C_2}{H_5}COOH > C{H_3}COOH\)
2 \(C{H_2}ClCOOH\;\; > HCOOH\;\; > \)\(C{H_3}COOH\;\; > {C_2}{H_5}COOH\)
3 \({C_2}{H_5}COOH\;\; > \;C{H_3}COOH\;\; > \)\(HCOOH\;\; > C{H_2}ClCOOH\)
4 \(HCOOH\;\; > C{H_2}ClCOOH\;\; > \)\(C{H_3}COOH\;\; > {C_2}{H_5}COOH\)
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ALDEHYDES, KETONES AND CARBOXYLIC ACID

28062 The fatty acid which shows reducing property is

1 Acetic acid
2 Ethanoic Acid
3 Oxalic acid
4 Formic acid
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28063 The reagent that can be used to distinguish between methanoic acid and ethanoic acid is

1 Ammoniacal silver nitrate solution
2 Neutral ferric Chloride solution
3 Sodium carbonate solution
4 Phenolphthalein
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28064 Hydrolysis of an ester gives acid \(A\) and alcohol \(B\). \(A\) reduces Fehling solution and oxidation of \(B\) gives \(A\). The ester is

1 Methyl formate
2 Ethyl formate
3 Methyl acetate
4 Ethyl acetate
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28065 Order of reactivity is

1 \(R - \mathop C\limits^{\mathop {||}\limits^O } - X\;\; > RCON{H_2}\;\; > RCOOCOR\;\; > RCOOR\)
2 \(RCOX\; > RCOOCOR\; > RCOOR\; > RCON{H_2}\)
3 \(RCOOR\; > RCON{H_2}\; > RCOX\; > RCOOCOR\)
4 \(RCOOCOR\; > RCOOR\; > RCOX\; > RCON{H_2}\)
ALDEHYDES, KETONES AND CARBOXYLIC ACID

28066 Right order of acidic strength is

1 \(C{H_2}ClCOOH > HCOOH > \)\({C_2}{H_5}COOH > C{H_3}COOH\)
2 \(C{H_2}ClCOOH\;\; > HCOOH\;\; > \)\(C{H_3}COOH\;\; > {C_2}{H_5}COOH\)
3 \({C_2}{H_5}COOH\;\; > \;C{H_3}COOH\;\; > \)\(HCOOH\;\; > C{H_2}ClCOOH\)
4 \(HCOOH\;\; > C{H_2}ClCOOH\;\; > \)\(C{H_3}COOH\;\; > {C_2}{H_5}COOH\)