Advertisements
Advertisements
Question
Choose the most correct option.
Which of the following compounds will dissolve in aqueous NaOH after undergoing reaction with Hinsberg reagent?
Options
Ethylamine
Triethylamine
Trimethylamine
Diethylamine
Advertisements
Solution
Ethylamine
APPEARS IN
RELATED QUESTIONS
How is ethyl amine prepared from methyl iodide?
Write a short note on Hoffmann bromamide degradation.
Illustrate the following reaction giving suitable example in each case:Gabriel phthalimide synthesis
An aromatic compound 'A' of molecular formula C7H7ON undergoes a series of reactions as shown below. Write the structures of A, B, C, D and E in the following reactions :

How do you convert the following: C6H5CONH2 to C6H5NH2
Give the structures of A, B and C in the following reactions :

Write a short note on the following:
Hoffmann’s bromamide reaction
Accomplish the following conversion:
Nitrobenzene to benzoic acid
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 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.
Give the structures of A, B and C in the following reactions :

Answer the following
Write a reaction to convert acetic acid into methylamine.
Write the order of reactivity of alkyl halides with ammonia.
Write reactions to bring about the following conversions.
Acetamide to methylamine
Why cannot aniline be prepared by Gabriel phthalimide synthesis?
____________ can be prepared exclusively by Gabriel phthalimide synthesis.
The reduction of alkyl cyanide with sodium and ethanol to give primary amines is, ____________.
Identify 'A' and 'B' in the following conversions.
\[\ce{CH3 - I ->[Alc. KCN][\Delta] A ->[Na/C2H5OH] B}\]
Which of the following amines cannot be prepared by Gabriel phthalimide synthesis?
Identify product B in the following reaction.
\[\ce{Aniline ->[NaNO2][HCl] A ->[KI] B}\]
Which of the following compounds is obtained when quaternary ammonium hydroxide is strongly heated?
Nitro compounds are reduced by iron scrap and hydrochloric acid to yield one of the following compounds:
Which of the following reagents would not be a good choice for reducing an aryl nitro compound to an amine?
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 ______.
The source of nitrogen in Gabriel synthesis of amines is ______.
Amongst the given set of reactants, the most appropriate for preparing 2° amine is ______.
The best reagent for converting 2–phenylpropanamide into 2-phenylpropanamine is ______.
The best reagent for converting, 2-phenylpropanamide into 1- phenylethanamine is ______.
Among the following amines, the strongest Brönsted base is:
Reduction of nitrobenzene by which of the following reagent gives aniline?
(i) \[\ce{Sn/HCl}\]
(ii) \[\ce{Fe/HCl}\]
(iii) \[\ce{H2 - Pd}\]
(iv) \[\ce{Sn/NH4OH}\]
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.\[\ce{H2 SO4}\].
Suggest a route by which the following conversion can be accomplished.

How will you bring out the following conversion?

How will you carry out the following conversions?

Match the reactions given in Column I with the statements given in Column II.
| Column I | Column II | ||
| (i) | Ammonolysis | (a) | Amine with lesser number of carbon atoms |
| (ii) | Gabriel phthalimide synthesis | (b) | Detection test for primary amines. |
| (iii) | Hoffmann Bromamide reaction | (c) | Reaction of phthalimide with \[\ce{KOH}\] and \[\ce{R-X}\] |
| (iv) | Carbylamine reaction | (d) | Reaction of alkylhalides with \[\ce{NH3}\] |
Account for the following:
Aniline cannot be prepared by the ammonolysis of chlorobenzene under normal conditions.
Reduction of nitro alkanes yields which compound?
C6H5CONHCH3 can be converted into C6H5CH2NHCH3 by:-
Which of the following CANNOT be prepared by ammonolysis of alkyl halide?
- Phenyl methenamine
- N, N - Dimethylaniline
- N - Methyl aniline
- Benzenamine
Choose the correct order of the basic nature of the above amines.
Which of the following statement(s) is/are incorrect in case of Hofmann bromamide degradation?
Amides can be converted into amines by the reaction named ______.
Identify the compo ds A and B in the following reactions:
\[\ce{A ->[Nitrating mixture] B ->[(i) Sn/cone. HCI][(ii) NaOH] Aniline}\]
Write short note on the following:
Ammonolysis
Write a short note on the following:
Ammonolysis
Write a short note on the following:
Ammonolysis
Write short note on the following.
Ammonolysis.
Write a short note on Ammonolysis.
Assertion: Amimonolysis of alkyl halides involves the reaction between alkyl halides and alcoholic ammonia.
Reason: Ammonolysis of alkyl halides produces secondary amines only.
Write a short note on the following:
Ammonolysis.
