Advertisements
Advertisements
प्रश्न
Identify A, B, C in the following reaction sequence:
\[\ce{CH3 - CH = CH2 ->[Br2/CCl4][room temperature] A ->[Zn] B ->[dil. alkaline][KMnO4] C}\]
Advertisements
उत्तर
\[\begin{array}{cc}
\ce{H\phantom{....}H\phantom{...............}}\\
|\phantom{.....}|\phantom{...............}\\
\ce{CH3\underset{Propene}{- CH =} CH2 ->[Br2/CCl4][room temperature] CH3 - C - C - H ->[Zn] CH3 \underset{\overset{Propene}{(B)}}{- CH = C}H2 ->[dil.alkaline][KMnO4] CH3 - CH - CH2}\\
\phantom{........................................}|\phantom{.....}|\phantom{..............................................}|\phantom{......}|\phantom{..}\\
\ce{\phantom{.......................................}\underset{\overset{1,2-Dibromopropane}{(A)}}{Br\phantom{...} Br}\phantom{...........................................}\underset{\overset{Propane-1,2-diol}{(C)}}{OH\phantom{...}OH}}\end{array}\]
APPEARS IN
संबंधित प्रश्न
Name the following:
The hydrocarbon said to possess carcinogenic property.
Predict the possible product of the following reaction.
bromination of phenol
Predict the possible product of the following reaction.
nitration of toluene
Identify the main product of the reaction:
\[\ce{H - C ≡ C - H + H - O ->[{40%} H2SO4][{1%} HgSO4]}\] _____.
Identify giving reason whether the following compound is aromatic or not.

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?
Major product of the below mentioned reaction is, \[\ce{(CH3 )2 C = CH2 ->[ICI]}\]
Consider the nitration of benzene using mixed con H2SO4 and HNO3 if a large quantity of KHSO4 is added to the mixture, the rate of nitration will be ______.
is
Some meta-directing substituents in aromatic substitution are given. Which one is most deactivating?
Give IUPAC name for the following compound.
Ethyl isopropyl acetylene
Suggest the route for the preparation of the following from benzene.
Bromo benzene
Write the structure of the following alkanes.
5 – (1, 2 – Dimethyl propyl) – 2 – methylnonane
When acetylene is passed through red hot iron tube at 873 K, ____________ is/are obtained as product/s.
Which among the following compounds has highest boiling point?
−Cl group is ____________.
According to Huckel rule, a cyclic π molecular orbital formed by overlap of p orbitals must contain ____________ p electrons.
Which of the following reagents can bring about following conversion?
\[\ce{But-1-ene -> Butan-2-ol}\]
Which of the following compounds on bromination yields
?
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.
\[\begin{array}{cc}
\phantom{..............................}\ce{CH3}\\
\phantom{............................}|\\
\ce{CH3 - C = CH2 + HBr ->[benzoyl][peroxide] CH3 - CH - CH2Br}\\
|\phantom{....................................}\\
\ce{CH_3}\phantom{.................................}
\end{array}\]
- 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.
Identify ortho and para-directing groups from the following:
\[\ce{\underset{I}{–CHO},\underset{II}{–NHCOCH3},\underset{III}{–OCH3},\underset{IV}{–SO3H}}\]
Which of the following is most stable?
