Advertisements
Advertisements
Questions
Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
(CH3CH2)2NCH3
Write the IUPAC name of the following compound:
(CH3CH2)2NCH3
Options
Primary
Secondary
Tertiary
Advertisements
Solution
Tertiary
IUPAC name: N-Ethyl-N-methylethanamine
Notes
Students should refer to the answer according to their questions.
RELATED QUESTIONS
Which among the following molecular formulae represents urotropine?
(a) C6H12N4
(b) C6H24H4
(c) C6H12N4O2
(d) C6H24N4O2
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(CH2)2NH2
Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
(CH3)3CNH2
Account for the following:
Ethylamine is soluble in water, whereas aniline is not.
Account for the following:
Methylamine in water reacts with ferric chloride to precipitate hydrated ferric oxide.
How will you convert methanol to ethanoic acid?
How will you convert ethanoic acid into propanoic acid?
An aromatic compound ‘A’ on treatment with aqueous ammonia and heating forms compound ‘B’ which on heating with Br2 and KOH forms a compound ‘C’ of molecular formula C6H7N. Write the structures and IUPAC names of compounds A, B and C.
Complete the following reaction:
\[\ce{C6H5NH2 + Br2 (aq) ->}\]
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
Do the following conversions in not more than two steps :
Ethyl benzene to Benzoic acid
What is the action of p-toluenesulphonychloride on ethylamine and diethylamine?
Give simple chemical tests to distinguish between the following pair of compounds:
Benzaldehyde and Benzoic acid
The following amine is called as:

Identify the incorrect IUPAC name.
Do the following conversions in not more than two steps:
\[\begin{array}{cc}
\ce{CH3CN to CH3 - C - CH3}\\
\phantom{...........}||\\
\phantom{...........}\ce{O}
\end{array}\]
