Advertisements
Advertisements
Question
Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
CH3(CH2)2NH2
Options
Primary
Secondary
Tertiary
Advertisements
Solution
Primary
IUPAC Name: Propan-1-amine
APPEARS IN
RELATED QUESTIONS
Convert 3-Methylaniline into 3-nitrotoluene.
Convert aniline into 1, 3, 5-tribromobenzene.
Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
CH3NHCH(CH3)2
Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
(CH3)3CNH2
Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
C6H5NHCH3
Give one chemical test to distinguish between the following pair of compounds.
Secondary and tertiary amines
Give one chemical test to distinguish between the following pair of compounds.
Ethylamine and aniline
Account for the following:
Methylamine in water reacts with ferric chloride to precipitate hydrated ferric oxide.
How will you convert hexanenitrile into 1-aminopentane?
How will you convert methanamine into ethanamine?
Accomplish the following conversion:
Benzoic acid to aniline
Accomplish the following conversion:
Aniline to 2, 4, 6-tribromofluorobenzene
Accomplish the following conversion:
Aniline to benzyl alcohol
Complete the following reaction:
\[\ce{C6H5NH2 + H2SO4 (conc.)}\]
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?
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:
\[\begin{array}{cc}
\ce{CH3CN to CH3 - C - CH3}\\
\phantom{...........}||\\
\phantom{...........}\ce{O}
\end{array}\]
