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Question
What is the action of p-toluenesulphonychloride on ethylamine and diethylamine?
Solution
It help to distinguish between primary and secondary amines
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RELATED QUESTIONS
Which among the following molecular formulae represents urotropine?
(a) C6H12N4
(b) C6H24H4
(c) C6H12N4O2
(d) C6H24N4O2
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Convert aniline into 1, 3, 5-tribromobenzene.
Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
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Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
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Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
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Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
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Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
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Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
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Give one chemical test to distinguish between the following pair of compounds.
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Account for the following:
Ethylamine is soluble in water whereas aniline is not.
How will you convert Hexanenitrile into 1-aminopentane
How will you convert Ethanamine into methanamine
How will you convert Ethanoic acid into propanoic acid
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Accomplish the following conversions - Aniline to 2,4,6-tribromofluorobenzene
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Complete the following reactions:
`C_6H_5NH_2 +H_2SO_4(conc.) ->`
Complete the following reactions:
Do the following conversions in not more than two steps :
Ethyl benzene to Benzoic acid
Give simple chemical tests to distinguish between the following pair of compounds:
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The following amine is called as:
An organic compound (A) with molecular formula C3H7NO on heating with Br2 and KOH forms a compound (B). Compound (B) on heating with CHCl3 and alcoholic KOH produces a foul-smelling compound (C) and on reacting with C6H5SO2Cl forms a compound (D) which is soluble in alkali. Write the structure of (A), (B), (C) and (D).
Do the following conversions in not more than two steps:
\[\begin{array}{cc}
\ce{CH3CN to CH3 - C - CH3}\\
\phantom{...........}||\\
\phantom{...........}\ce{O}
\end{array}\]
