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An organic compound A (c3h7no) on hydrolysis give amine B and a carboxylic acid C .amine B reacts with benzenesulphonyl chloride and gives a product which is insoluble in aqueous sodium hydroxide solution.acid C on reaction with tollen's reagent gives a silver mirror .write the structure of A,B and C. Plzz give me answer in quick.it's my request?
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An organic compound A (c3h7no) on hydrolysis give amine B and a carbox...
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An organic compound A (c3h7no) on hydrolysis give amine B and a carbox...
Structure of Compound A (C3H7NO):
Compound A is an organic compound with the molecular formula C3H7NO. To determine the structure of A, we need to consider its hydrolysis products and the given information.
Hydrolysis of Compound A:
When Compound A undergoes hydrolysis, it forms amine B and carboxylic acid C. This suggests that Compound A is an amide. The hydrolysis reaction can be represented as follows:
C3H7NO + H2O → C3H7NH2 + C3H6O2
Reaction of Amine B with Benzenesulphonyl Chloride:
Amine B reacts with benzenesulphonyl chloride (C6H5SO2Cl) to form an insoluble product. This reaction is known as a sulfonation reaction. The reaction can be represented as follows:
C3H7NH2 + C6H5SO2Cl → Insoluble Product
Reaction of Acid C with Tollen's Reagent:
When carboxylic acid C reacts with Tollen's reagent (ammoniacal silver nitrate), it forms a silver mirror. This reaction indicates the presence of an aldehyde group in acid C. The reaction can be represented as follows:
C3H6O2 + 2Ag(NH3)2OH → Silver Mirror
Structure of Compound A:
From the given information, Compound A is an amide. The structure of Compound A can be represented as follows:
H3C-C(=O)-NH-CH2CH3
Structure of Amine B:
Amine B is formed from Compound A upon hydrolysis. It can be represented as follows:
H3C-CH(NH2)-CH2CH3
Structure of Carboxylic Acid C:
Carboxylic acid C is formed from Compound A upon hydrolysis. It contains an aldehyde group, as indicated by the silver mirror test. The structure of acid C can be represented as follows:
H3C-CH2-CHO
To summarize:
- Compound A is an amide (C3H7NO) that hydrolyzes to form amine B and carboxylic acid C.
- Amine B reacts with benzenesulphonyl chloride to form an insoluble product.
- Carboxylic acid C gives a silver mirror when reacted with Tollen's reagent, indicating the presence of an aldehyde group.
- The structures of Compound A, amine B, and carboxylic acid C are H3C-C(=O)-NH-CH2CH3, H3C-CH(NH2)-CH2CH3, and H3C-CH2-CHO, respectively.
Compound A is an organic compound with the molecular formula C3H7NO. To determine the structure of A, we need to consider its hydrolysis products and the given information.
Hydrolysis of Compound A:
When Compound A undergoes hydrolysis, it forms amine B and carboxylic acid C. This suggests that Compound A is an amide. The hydrolysis reaction can be represented as follows:
C3H7NO + H2O → C3H7NH2 + C3H6O2
Reaction of Amine B with Benzenesulphonyl Chloride:
Amine B reacts with benzenesulphonyl chloride (C6H5SO2Cl) to form an insoluble product. This reaction is known as a sulfonation reaction. The reaction can be represented as follows:
C3H7NH2 + C6H5SO2Cl → Insoluble Product
Reaction of Acid C with Tollen's Reagent:
When carboxylic acid C reacts with Tollen's reagent (ammoniacal silver nitrate), it forms a silver mirror. This reaction indicates the presence of an aldehyde group in acid C. The reaction can be represented as follows:
C3H6O2 + 2Ag(NH3)2OH → Silver Mirror
Structure of Compound A:
From the given information, Compound A is an amide. The structure of Compound A can be represented as follows:
H3C-C(=O)-NH-CH2CH3
Structure of Amine B:
Amine B is formed from Compound A upon hydrolysis. It can be represented as follows:
H3C-CH(NH2)-CH2CH3
Structure of Carboxylic Acid C:
Carboxylic acid C is formed from Compound A upon hydrolysis. It contains an aldehyde group, as indicated by the silver mirror test. The structure of acid C can be represented as follows:
H3C-CH2-CHO
To summarize:
- Compound A is an amide (C3H7NO) that hydrolyzes to form amine B and carboxylic acid C.
- Amine B reacts with benzenesulphonyl chloride to form an insoluble product.
- Carboxylic acid C gives a silver mirror when reacted with Tollen's reagent, indicating the presence of an aldehyde group.
- The structures of Compound A, amine B, and carboxylic acid C are H3C-C(=O)-NH-CH2CH3, H3C-CH(NH2)-CH2CH3, and H3C-CH2-CHO, respectively.
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An organic compound A (c3h7no) on hydrolysis give amine B and a carboxylic acid C .amine B reacts with benzenesulphonyl chloride and gives a product which is insoluble in aqueous sodium hydroxide solution.acid C on reaction with tollen's reagent gives a silver mirror .write the structure of A,B and C. Plzz give me answer in quick.it's my request?
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An organic compound A (c3h7no) on hydrolysis give amine B and a carboxylic acid C .amine B reacts with benzenesulphonyl chloride and gives a product which is insoluble in aqueous sodium hydroxide solution.acid C on reaction with tollen's reagent gives a silver mirror .write the structure of A,B and C. Plzz give me answer in quick.it's my request? for NEET 2024 is part of NEET preparation. The Question and answers have been prepared according to the NEET exam syllabus. Information about An organic compound A (c3h7no) on hydrolysis give amine B and a carboxylic acid C .amine B reacts with benzenesulphonyl chloride and gives a product which is insoluble in aqueous sodium hydroxide solution.acid C on reaction with tollen's reagent gives a silver mirror .write the structure of A,B and C. Plzz give me answer in quick.it's my request? covers all topics & solutions for NEET 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for An organic compound A (c3h7no) on hydrolysis give amine B and a carboxylic acid C .amine B reacts with benzenesulphonyl chloride and gives a product which is insoluble in aqueous sodium hydroxide solution.acid C on reaction with tollen's reagent gives a silver mirror .write the structure of A,B and C. Plzz give me answer in quick.it's my request?.
An organic compound A (c3h7no) on hydrolysis give amine B and a carboxylic acid C .amine B reacts with benzenesulphonyl chloride and gives a product which is insoluble in aqueous sodium hydroxide solution.acid C on reaction with tollen's reagent gives a silver mirror .write the structure of A,B and C. Plzz give me answer in quick.it's my request? for NEET 2024 is part of NEET preparation. The Question and answers have been prepared according to the NEET exam syllabus. Information about An organic compound A (c3h7no) on hydrolysis give amine B and a carboxylic acid C .amine B reacts with benzenesulphonyl chloride and gives a product which is insoluble in aqueous sodium hydroxide solution.acid C on reaction with tollen's reagent gives a silver mirror .write the structure of A,B and C. Plzz give me answer in quick.it's my request? covers all topics & solutions for NEET 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for An organic compound A (c3h7no) on hydrolysis give amine B and a carboxylic acid C .amine B reacts with benzenesulphonyl chloride and gives a product which is insoluble in aqueous sodium hydroxide solution.acid C on reaction with tollen's reagent gives a silver mirror .write the structure of A,B and C. Plzz give me answer in quick.it's my request?.
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An organic compound A (c3h7no) on hydrolysis give amine B and a carboxylic acid C .amine B reacts with benzenesulphonyl chloride and gives a product which is insoluble in aqueous sodium hydroxide solution.acid C on reaction with tollen's reagent gives a silver mirror .write the structure of A,B and C. Plzz give me answer in quick.it's my request?, a detailed solution for An organic compound A (c3h7no) on hydrolysis give amine B and a carboxylic acid C .amine B reacts with benzenesulphonyl chloride and gives a product which is insoluble in aqueous sodium hydroxide solution.acid C on reaction with tollen's reagent gives a silver mirror .write the structure of A,B and C. Plzz give me answer in quick.it's my request? has been provided alongside types of An organic compound A (c3h7no) on hydrolysis give amine B and a carboxylic acid C .amine B reacts with benzenesulphonyl chloride and gives a product which is insoluble in aqueous sodium hydroxide solution.acid C on reaction with tollen's reagent gives a silver mirror .write the structure of A,B and C. Plzz give me answer in quick.it's my request? theory, EduRev gives you an
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