Advertisements
Advertisements
प्रश्न
Predict the possible product of the following reaction.
Chlorination of nitrobenzene
Advertisements
उत्तर
The Nitro group is a meta directing group. So, chlorination of nitrobenzene gives m-chloronitrobenzene.

APPEARS IN
संबंधित प्रश्न
Write the balanced chemical reaction to get benzene from Sodium benzoate.
Predict the possible product of the following reaction.
nitration of toluene
Identify giving reason whether the following compound is aromatic or not.

Read the following reaction and answer the questions given below:

- Write the name of the reaction.
- Identify the electrophile in it.
- How is this electrophile generated?
Which of the following compounds will not undergo Friedal – crafts reaction easily ? (NEET)
Identify the compound A, B, C and D in the following series of reactions.

Write short notes on ortho, para directors in aromatic electrophilic substitution reactions.
Suggest the route for the preparation of the following from benzene.
m - dinitro benzene
How will you convert ethyl chloride into ethane?
Write the structure of the following alkanes.
5 – (1, 2 – Dimethyl propyl) – 2 – methylnonane
How will distinguish 1 – butyne and 2 – butyne?
Which of the following is an aromatic compound?
When acetylene is passed through red hot iron tube at 873 K, ____________ is/are obtained as product/s.
Phenol on distillation with zinc dust gives ____________.
According to Huckel rule, a cyclic π molecular orbital formed by overlap of p orbitals must contain ____________ p electrons.
Which of the following is INCORRECT for aromatic hydrocarbons?
The alkane formed on heating sodium butanoate with sodalime is ______.
Sodium benzoate on decarboxylation gives ____________.
Dow's process is used for the synthesis of an aromatic compound (X). Identify X.
Which of the following molecules has shortest C - C bond length?
The treatment of benzene with iso - butene in the presence of sulphuric acid gives:
Conversion of hexane into benzene involves the reaction of ______.
Read the following reaction and answer the questions given below.
\[\begin{array}{cc}
\phantom{..............................}\ce{CH3}\\
\phantom{...........................}|\\
\ce{CH3 - C = CH2 + HBr ->[Benzoyl][peroxide] H3C - CH - CH2Br}\\
|\phantom{....................................}\\
\ce{CH3}\phantom{.................................}
\end{array}\]
- Write the IUPAC name of the product.
- State the rule that governs the formation of this product.
Read the following reaction and answer the questions given below.
\[\begin{array}{cc}
\phantom{.............................}\ce{CH3}\\
\phantom{...........................}|\\
\ce{CH3 - C = CH2 + HBr ->[benzoyl][peroxide] CH3 - CH - CH2Br}\\
|\phantom{....................................}\\
\ce{CH3}\phantom{.................................}\\
\end{array}\]
- Write IUPAC name of the product.
- State the rule that governs formation of this product.
Read the following reaction and answer the questions given below.
\[\begin{array}{cc}
\phantom{..............................}\ce{CH3}\\
\phantom{...........................}|\\
\ce{CH3 - C = CH2 + HBr ->[benzoyl][peroxide] CH3 - CH - CH2Br}\\
|\phantom{....................................}\\
\ce{CH3}\phantom{.................................}
\end{array}\]
- Write the IUPAC name of the product.
- State the rule that governs the formation of this product.
Read the following reaction and answer the questions given below.
\[\begin{array}{cc}
\phantom{...............................}\ce{CH3}\\
\phantom{............................}|\\
\ce{CH3 - C = CH2 + HBr ->[benzoyl][peroxide]CH3 - CH - CH2Br}\\
|\phantom{....................................}\\
\ce{CH3}\phantom{..................................}
\end{array}\]
- Write the IUPAC name of the product.
- State the rule that governs the formation of this product.
Identify 'A' in the following reaction.
\[\ce{\underset{}{A + Chloromethane} ->[anhydrous][AlCl3] \underset{\underset{}{}}{2-Chlorotoluene + 4-Chlorotoluene}}\]
Identify ortho and para-directing groups from the following:
\[\ce{\underset{I}{–CHO},\underset{II}{–NHCOCH3},\underset{III}{–OCH3},\underset{IV}{–SO3H}}\]
