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प्रश्न
How will you carry out the following conversion?
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उत्तर
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संबंधित प्रश्न
Give a plausible explanation for the following:
Why are amines less acidic than alcohols of comparable molecular masses?
The following amines is the product of Gabriel phthalimide synthesis.
Name the process of breaking C-X bond by ammonia in preparation of amines.
Acetamide on reduction using Na/C2H5OH gives ____________.
Which of the following amines forms a clear solution when treated with benzene sulphonyl chloride and excess of potassium hydroxide?
Identify 'A' and 'B' in the following conversions.
\[\ce{CH3 - I ->[Alc. KCN][\Delta] A ->[Na/C2H5OH] B}\]
In aqueous phase the order of basic strength of alkylamine is ______.
Identify product B in the following reaction.
\[\ce{Aniline ->[NaNO2][HCl] A ->[KI] B}\]
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?
Reduction of aromatic nitro compounds using \[\ce{Fe}\] and \[\ce{HCl}\] gives ______.
Which of the following methods of preparation of amines will give same number of carbon atoms in the chain of amines as in the reactant?
How will you bring out the following conversion?
How will you carry out the following conversion?
Describe Gabriel's phthalimide synthesis. (Give reaction)
Account for the following:
Aniline cannot be prepared by the ammonolysis of chlorobenzene under normal conditions.
The Gabriels' phthalimide synthesis is used in the synthesis of
Which of the following amines can be prepared by Gabriel phthalimide reaction?
Identify A and B in the following reaction.
\[\ce{C6H5CH2Br ->[Alco.][KCN] A ->[Na/Ethanol][reduction] B}\]
Write short note on the following.
Ammonolysis.
