Accomplish the conversion : Chlorobenzene to p-chloroamine - Vidyadip

Question

Accomplish the conversion :
Chlorobenzene to p-chloroamine

✓

Answer

Get the step-by-step solution for this question inside the Vidyadip app.

Get the answer in the app

Need a full question paper?

Generate a complete, print-ready paper with questions like this in minutes — across 16+ boards, with answer keys.

Start Generating Free

Explore more

More "1 Marks Question" from Amines→Amines — all question types→Chemistry STD 12 Science question papers→Rajasthan Board STD 12 Science question papers→Rajasthan Board question paper generator→

Similar questions

Draw structure of the derivative :
The methyl hemiacetal of formaldehyde.

Name the following halides according to $\text{IUPAC}$ system and classify them as alkyl, allyl, benzyl $($primary, secondary, tertiary$),$ vinyl or aryl halides: $\ce{CH_3CH_2CH(CH_3)CH(C_2H_5)Cl}.$

What will be the effect on the rate of a zero order reaction if the concentration of reactant is tripled?

Write the structure of the major organic product in each of the following reaction:
$\text{CH}_3\text{CH}_2\text{Br}+\text{KCN}\xrightarrow{\text{aq. ethanol}}$

In an aqueous solution how does specific conductivity of electrolytes change with addition of water?

Account for the following :
Ethyl amine is soluble in water whereas aniline is not.

Read the given passage and answer the questions number $1$ to $5$ that follow:
The substitution reaction of alkyl halide mainly occurs by $S_N1$ or $S_N2$ mechanism. Whatever mechanism alkyl halides follow for the substitution reaction to occur, the polarity of the carbon halogen bond is responsible for these substitution reactions. The rate of $S_N1$ reactions are governed by the stability of carbocation whereas for $S_N2$ reactions steric factor is the deciding factor. If the starting material is a chiral compound, we may end up with an inverted product or racemic mixture depending upon the type of mechanism followed by alkyl halide. Cleavage of ethers with $HI$ is also governed by steric factor and stability of carbocation, which indicates that in organic chemistry, these two major factors help us in deciding the kind of product formed.
Predict the stereochemistry of the product formed if an optically active alkyl halide undergoes substitution reaction by $S_N1$ mechanism.

Account for the following :
Aniline does not undergo Friedel-Crafts reaction.

What is the order of decomposition of $N _2 O _5$ ?

Describe the following:Decarboxylation.