28469
Formic acid and acetic acid can be distinguished by
1 Tollen's reagent
2 \(NaHCO_3\)
3 Litmus test
4 \(Na\)
Explanation:
Formic acid has aldehyde group. It reduces Tollen's reagent to silver mirror like other aldehydes. Tollen's test is not given by Carboxylic acids.
ALDEHYDES, KETONES AND CARBOXYLIC ACID
28470
The major product in the reaction
1
2
3
4
Explanation:
ALDEHYDES, KETONES AND CARBOXYLIC ACID
28471
(image) \(\xrightarrow{{electrolysis}}X\xrightarrow[{H{g^{ + 2}}}]{{dil.{H_2}S{O_4}}}Y;\,Y\) is
1 \(CH_3-CH=O\)
2 \(CH_3-CH_2-OH\)
3 \(CH_3-CH_2-CH=O\)
4 \(CH_3-CH_2-CH_2-OH\)
Explanation:
ALDEHYDES, KETONES AND CARBOXYLIC ACID
28472
In following given reaction\(CH_3COOH + PCl_5 \longrightarrow (A)\) \(\xrightarrow[(2){{H}_{2}}O]{(1)\,C{{H}_{3}}MgBr}\left( B \right)\) Product \(B\) would be
28469
Formic acid and acetic acid can be distinguished by
1 Tollen's reagent
2 \(NaHCO_3\)
3 Litmus test
4 \(Na\)
Explanation:
Formic acid has aldehyde group. It reduces Tollen's reagent to silver mirror like other aldehydes. Tollen's test is not given by Carboxylic acids.
ALDEHYDES, KETONES AND CARBOXYLIC ACID
28470
The major product in the reaction
1
2
3
4
Explanation:
ALDEHYDES, KETONES AND CARBOXYLIC ACID
28471
(image) \(\xrightarrow{{electrolysis}}X\xrightarrow[{H{g^{ + 2}}}]{{dil.{H_2}S{O_4}}}Y;\,Y\) is
1 \(CH_3-CH=O\)
2 \(CH_3-CH_2-OH\)
3 \(CH_3-CH_2-CH=O\)
4 \(CH_3-CH_2-CH_2-OH\)
Explanation:
ALDEHYDES, KETONES AND CARBOXYLIC ACID
28472
In following given reaction\(CH_3COOH + PCl_5 \longrightarrow (A)\) \(\xrightarrow[(2){{H}_{2}}O]{(1)\,C{{H}_{3}}MgBr}\left( B \right)\) Product \(B\) would be
28469
Formic acid and acetic acid can be distinguished by
1 Tollen's reagent
2 \(NaHCO_3\)
3 Litmus test
4 \(Na\)
Explanation:
Formic acid has aldehyde group. It reduces Tollen's reagent to silver mirror like other aldehydes. Tollen's test is not given by Carboxylic acids.
ALDEHYDES, KETONES AND CARBOXYLIC ACID
28470
The major product in the reaction
1
2
3
4
Explanation:
ALDEHYDES, KETONES AND CARBOXYLIC ACID
28471
(image) \(\xrightarrow{{electrolysis}}X\xrightarrow[{H{g^{ + 2}}}]{{dil.{H_2}S{O_4}}}Y;\,Y\) is
1 \(CH_3-CH=O\)
2 \(CH_3-CH_2-OH\)
3 \(CH_3-CH_2-CH=O\)
4 \(CH_3-CH_2-CH_2-OH\)
Explanation:
ALDEHYDES, KETONES AND CARBOXYLIC ACID
28472
In following given reaction\(CH_3COOH + PCl_5 \longrightarrow (A)\) \(\xrightarrow[(2){{H}_{2}}O]{(1)\,C{{H}_{3}}MgBr}\left( B \right)\) Product \(B\) would be
28469
Formic acid and acetic acid can be distinguished by
1 Tollen's reagent
2 \(NaHCO_3\)
3 Litmus test
4 \(Na\)
Explanation:
Formic acid has aldehyde group. It reduces Tollen's reagent to silver mirror like other aldehydes. Tollen's test is not given by Carboxylic acids.
ALDEHYDES, KETONES AND CARBOXYLIC ACID
28470
The major product in the reaction
1
2
3
4
Explanation:
ALDEHYDES, KETONES AND CARBOXYLIC ACID
28471
(image) \(\xrightarrow{{electrolysis}}X\xrightarrow[{H{g^{ + 2}}}]{{dil.{H_2}S{O_4}}}Y;\,Y\) is
1 \(CH_3-CH=O\)
2 \(CH_3-CH_2-OH\)
3 \(CH_3-CH_2-CH=O\)
4 \(CH_3-CH_2-CH_2-OH\)
Explanation:
ALDEHYDES, KETONES AND CARBOXYLIC ACID
28472
In following given reaction\(CH_3COOH + PCl_5 \longrightarrow (A)\) \(\xrightarrow[(2){{H}_{2}}O]{(1)\,C{{H}_{3}}MgBr}\left( B \right)\) Product \(B\) would be