Advertisements
Advertisements
प्रश्न
Predict the possible product of the following reaction.
sulphonation of chlorobenzene
Advertisements
उत्तर
Chloro group is ortho and para directing group. So, sulphonation of chlorobenzene gives p-chlorobenzene sulphonic acid and o- chlorobenzene sulphonic acid.
APPEARS IN
संबंधित प्रश्न
Predict the possible product of the following reaction.
bromination of phenol
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?
Identify the compound 'Z' in the following reaction
\[\ce{C2H6O ->[Al2O3][623 K] X ->[O3] Y ->[Zn/H2O] (Z)}\]
How does Huckel rule help to decide the aromatic character of a compound?
Suggest the route for the preparation of the following from benzene.
3 – chloro nitrobenzene
Suggest the route for the preparation of the following from benzene.
Bromo benzene
Suggest the route for the preparation of the following from benzene.
m - dinitro benzene
Write the structure of the following alkanes.
2, 3 – Dimethyl – 6 – (2 – methyl propyl) decane
Write the structure of the following alkanes.
5 – (2 – Ethyl butyl) – 3, 3 – dimethyldecane
Complete the following:
\[\begin{array}{cc}
\ce{CH2 - CH2 ->[Zn/C2H5OH]}\\
|\phantom{.......}|\phantom{..............}\\
\ce{Br}\phantom{.....}\ce{Br}\phantom{..............}
\end{array}\]
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.
Direct bromination of benzene with excess reagent results in the formation of ____________.
Dow's process is used for the synthesis of an aromatic compound (X). Identify X.
The treatment of benzene with iso - butene in the presence of sulphuric acid gives:
Arenes on treatments with chlorine in the presence of ferric chloride as a catalyst undergo what type of reaction?
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.
\[\begin{array}{cc}
\phantom{..............................}\ce{CH3}\\
\phantom{...........................}|\\
\ce{CH3 - C = CH2 + HBr->[Benzoyl][peroxide] H3C - CH - CH2Br}\\
|\phantom{....................................}\\
\ce{CH3}\phantom{.................................}
\end{array}\]
- 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.
\[\begin{array}{cc}
\phantom{..............................}\ce{CH3}\\
\phantom{............................}|\\
\ce{CH3 - C = CH2 + HBr ->[benzoyl][peroxide] CH3 - CH - CH2Br}\\
|\phantom{....................................}\\
\ce{CH_3}\phantom{.................................}
\end{array}\]
- 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.
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.
Identify ortho and para-directing groups from the following:
\[\ce{\underset{I}{–CHO},\underset{II}{–NHCOCH3},\underset{III}{–OCH3},\underset{IV}{–SO3H}}\]
