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कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

Complete the following reaction: C6H5NH2 + Br2 (aq) ->

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प्रश्न

Complete the following reaction:

\[\ce{C6H5NH2 + Br2 (aq) ->}\]

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उत्तर

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पाठ 9: Amines - Exercises [पृष्ठ २८०]

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एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
पाठ 9 Amines
Exercises | Q 9.11 (v) | पृष्ठ २८०

संबंधित प्रश्‍न

Convert aniline into 1, 3, 5-tribromobenzene.


Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.

(CH3)2CHNH2


Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.

(CH3)3CNH2


Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.

m−BrC6H4NH2


Give one chemical test to distinguish between the following pair of compounds.

Methylamine and dimethylamine


Give one chemical test to distinguish between the following pair of compounds.

Ethylamine and aniline


Give one chemical test to distinguish between the following pair of compounds.

Aniline and benzylamine


Account for the following:

pKb of aniline is more than that of methylamine.


How will you convert methanol to ethanoic acid?


How will you convert ethanamine into methanamine?


How will you convert methanamine into ethanamine?


Accomplish the following conversion:

Chlorobenzene to p-chloroaniline


Accomplish the following conversion:

Aniline to benzyl alcohol


Complete the following reaction:

\[\ce{C6H5NH2 + H2SO4 (conc.)}\]


Complete the following reaction:

\[\ce{C6H5NH2 + (CH3CO)2O ->}\]


Complete the following reaction:

\[\ce{C6H5N2Cl ->[(i) HBF4][(ii) NaNO2/Cu, \Delta]}\]


Give reasons  Although –NH2 is o/p directing group, yet aniline on nitration gives a significant amount of m-nitroaniline


How are ethylamine and ethyl methyl amine distinguished by using nitrous acid?


Give simple chemical tests to distinguish between the following pair of compounds:

Benzaldehyde and Benzoic acid


Do the following conversions in not more than two steps:

\[\begin{array}{cc}
\ce{CH3CN to CH3 - C - CH3}\\
\phantom{...........}||\\
\phantom{...........}\ce{O}
\end{array}\]


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