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Give the structure of A, B and C in the following reaction: {C6H5N2Cl ->[CuCN] A ->[H2O/H+] B ->[NH3][\Delta] C - Chemistry

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प्रश्न

Give the structure of A, B and C in the following reaction:

\[\ce{C6H5N2Cl ->[CuCN] A ->[H2O/H+] B ->[NH3][\Delta] C}\]

रासायनिक समीकरण/संरचनाएँ

उत्तर

\[\ce{\underset{chloride}{\underset{Benzenediazonium}{C6H5N2Cl}} ->[CuCN] \underset{(A)}{\underset{Cyanobenzene}{C6H5CN}} ->[H2O/H+] \underset{(B)}{\underset{Benzoic acid}{C6H5COOH}} ->[NH3][\Delta] \underset{(C)}{\underset{Benzamide}{C6H5CONH2}}}\]

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अध्याय 13: Amines - Exercises [पृष्ठ ४०१]

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एनसीईआरटी Chemistry [English] Class 12
अध्याय 13 Amines
Exercises | Q 9.2 | पृष्ठ ४०१

संबंधित प्रश्न

Illustrate the following reaction giving suitable example in each case:Gabriel phthalimide synthesis


Give the structures of A, B and C in the following reactions :


Explain the mechanism of action of hydroiodic acid on 3-methylbutan-2-ol.


Explain Hoffmann’s exhaustive alkylation with suitable reactions.


Write reactions for the preparation of ethanamine using Gabriel phthalimide synthesis.


Identify the major product (B).


What is the molar mass of the amine formed when acetamide undergoes Hofmann bromamide degradation?


Which nitrogen containing compound amongst the following would undergo Mendius reduction to furnish primary amine \[\ce{(R - NH2)}\]?


Which of the following amines cannot be prepared by Gabriel phthalimide synthesis?


In order to prepare a 1° amine from an alkyl halide with simultaneous addition of one \[\ce{CH2}\] group in the carbon chain, the reagent used as source of nitrogen is ______.


Best method for preparing primary amines from alkyl halides without changing the number of carbon atoms in the chain is ______.


Which of the following amines can be prepared by Gabriel synthesis.

(i) Isobutyl amine

(ii) 2-Phenylethylamine

(iii) N-methylbenzylamine

(iv) Aniline


Which of the following reactions are correct?

(i)

(ii)

(iii)

(iv)


Under which of the following reaction conditions, aniline gives p-nitro derivative as the major product?

(i) Acetyl chloride/pyridine followed by reaction with conc.\[\ce{H2SO4 }\] + conc. \[\ce{HNO3}\].

(ii) Acetic anyhdride/pyridine followed by conc.\[\ce{H2SO4}\] + conc.\[\ce{HNO3}\].

(iii) Dil. HCl followed by reaction with conc.\[\ce{H2SO4}\] + conc.\[\ce{HNO3}\].

(iv) Reaction with conc.\[\ce{HNO3}\] + conc.\[\ce{H2 SO4}\].


What is the product when \[\ce{C6H5CH2NH2}\] reacts with \[\ce{HNO2}\]?


Assertion: Only a small amount of \[\ce{HCl}\] is required in the reduction of nitro compounds with iron scrap and \[\ce{HCl}\] in the presence of steam.

Reason: \[\ce{FeCl2}\] formed gets hydrolysed to release \[\ce{HCl}\] during the reaction.


Assertion: Aromatic 1° amines can be prepared by Gabriel Phthalimide Synthesis.

Reason: Aryl halides undergo nucleophilic substitution with anion formed by phthalimide.


Describe Gabriel's phthalimide synthesis. (Give reaction)


In the given reaction what is the X?

\[\begin{array}{cc}
\ce{O}\phantom{.......................}\\
||\phantom{.......................}\\
\phantom{}\ce{R - C - OH <-[H3O] Χ ->[H] RCH2NH2}
\end{array}\]


Which of the following would not be a good choice for reducing nitrobenzene to aniline?


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