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प्रश्न
Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
m−BrC6H4NH2
पर्याय
Primary
Secondary
Tertiary
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उत्तर
Primary
IUPAC name: 3-Bromobenzenamine or 3-Bromoaniline
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संबंधित प्रश्न
Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
(CH3)2CHNH2
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.
CH3NHCH(CH3)2
Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
(CH3CH2)2NCH3
Give one chemical test to distinguish between the following pair of compounds.
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Give one chemical test to distinguish between the following pair of compounds.
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Give one chemical test to distinguish between the following pair of compounds.
Aniline and benzylamine
How will you convert ethanoic acid into methanamine?
How will you convert ethanamine into methanamine?
How will you convert methanamine into ethanamine?
How will you convert propanoic acid into ethanoic acid?
Accomplish the following conversion:
Chlorobenzene to p-chloroaniline
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:
\[\ce{C6H5NH2 + H2SO4 (conc.)}\]
Complete the following reaction:
\[\ce{C6H5N2Cl + C2H5OH ->}\]
Using IUPAC norms, write the formula of Hexaamminecobalt(III) sulphate.
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:
\[\begin{array}{cc}
\ce{CH3CN to CH3 - C - CH3}\\
\phantom{...........}||\\
\phantom{...........}\ce{O}
\end{array}\]
