Advertisements
Advertisements
प्रश्न
Answer the following
Identify A and B in the following reactions.
\[\ce{C6H5CH2Br->[alco.][KCN]A ->[Na/ethanol]B.}\]
Advertisements
उत्तर
\[\ce{\underset{\text{Benzyl bromide}}{C6H5 - CH2 - Br} ->[alcoholic KCN]\underset{\text{Phenylacetonitrile} (A)}{C6H5 - CH2 - C ≡ N} ->[Na/ethanol]\underset{\text{2-Phenylethylamine} (B)}{C6H5 - CH2 - CH2 - NH2}}\]
APPEARS IN
संबंधित प्रश्न
How is ethyl amine prepared from methyl iodide?
Write a short note on Hoffmann bromamide degradation.
Identify the compounds 'A' and 'B' in the following equation:
Give the structures of A, B and C in the following reactions :
Accomplish the following conversion:
Benzyl chloride to 2-phenylethanamine
Accomplish the following conversion:
Benzamide to toluene
Give the structure of A, B and C in the following reaction:
\[\ce{CH3CH2I ->[NaCN] A ->[OH-][Partial hydrolysis] B ->[NaOH + Br2] C}\]
Give the structure of A, B and C in the following reaction:
\[\ce{C6H5N2Cl ->[CuCN] A ->[H2O/H+] B ->[NH3][\Delta] C}\]
Give the structure of A, B and C in the following reaction:
\[\ce{C6H5NO2 ->[Fe/HCl] A ->[NaNO2 + HCl][273 K] B ->[H2O/H+][\Delta] C}\]
Give the structures of A, B and C in the following reaction:
\[\ce{C6H5NO2 ->[Fe/HCl] A ->[HNO2][273 K] B ->[C6H5OH] C}\]
Write the reaction of aromatic primary amine with nitrous acid.
Write the reaction of aliphatic primary amine with nitrous acid.
Arrange the following in the increasing order of their pKb values:
C6H5NH2, C2H5NH2, C6H5NHCH3
Give the structures of A, B and C in the following reactions :
Account for the following:
Gabriel phthalimide synthesis is not preferred for preparing aromatic primary amines.
Choose the most correct option.
Which of the following compounds will dissolve in aqueous NaOH after undergoing reaction with Hinsberg reagent?
Answer the following
Write a reaction to convert acetic acid into methylamine.
Answer the following
Explain Gabriel phthalimide synthesis.
Write reactions for the preparation of ethanamine using Gabriel phthalimide synthesis.
Explain the following reaction with a suitable example.
Hofmann elimination reaction
Identify compound 'B' in following series of reactions?
\[\ce{Acetonitrile ->[Na/alcohol] A ->[NaNO2/dil.HCI] B}\]
Acetamide on reduction using Na/C2H5OH gives ____________.
Identify the product 'A' in the following reaction.
\[\ce{Aniline ->[(CH3CO)2O][Pyridine] A}\]
Alkyl cyanides on reduction by sodium and ethanol give primary amines. This reaction is called as ____________.
Identify the product obtained when benzyl chloride undergoes ammonolysis in presence of excess ammonia followed by the reaction with two moles of methyl iodide.
\[\ce{CH3-CN ->[Na/C2H5OH]}\]
The product formed is ____________.
Which of the following reactions is appropriate for converting benzamide to aniline?
Identify 'A' and 'B' in the following conversions.
\[\ce{CH3 - I ->[Alc. KCN][\Delta] A ->[Na/C2H5OH] B}\]
Which of the following does NOT give carbylamine test?
Which of the following reactions does NOT yield an amine?
Given below are two statements labelled as Assertion (A) and Reason (R).
Assertion (A): Alkyl halides are insoluble in water.
Reason (R): Alkyl halides have halogen attached to sp3 hybrid carbon.
Select the most appropriate answer from the options given below:
Which of the following reagents would not be a good choice for reducing an aryl nitro compound to an amine?
Amongst the given set of reactants, the most appropriate for preparing 2° amine is ______.
The best reagent for converting, 2-phenylpropanamide into 1- phenylethanamine is ______.
Which of the following compounds is the weakest Brönsted base?
Among the following amines, the strongest Brönsted base 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)
What is the product when \[\ce{C6H5CH2NH2}\] reacts with \[\ce{HNO2}\]?
What is the best reagent to convert nitrile to primary amine?
Write following conversions:
acetanilide `->` p-nitroaniline
How will you bring out the following conversion?
Assertion: Hoffmann’s bromamide reaction is given by primary amines.
Reason: Primary amines are more basic than secondary amines.
The Gabriels' phthalimide synthesis is used in the synthesis of
In the given reaction what is the X?
\[\begin{array}{cc}
\ce{O}\phantom{.......................}\\
||\phantom{.......................}\\
\phantom{}\ce{R - C - OH <-[H3O] Χ ->[H] RCH2NH2}
\end{array}\]
Give reasons for the following:
Ammonolysis of alkyl halides is not a good method to prepare pure primary amines.
Methyl amine on reaction with chloroform in the presence of NaOH gives ______.
Which of the following amines can be prepared by Gabriel phthalimide reaction?
What is the IUPAC name of \[\ce{(CH3)2 - N - CH3}\]?
Write the name of the product formed by the action of LiAlH4/ether on acetamide.
Write a short note on the following:
Ammonolysis
Write the name of reduction product formed when ethyl cyanide is treated with sodium and alcohol.
Write a short note on Ammonolysis.
