Advertisements
Advertisements
Question
Complete the following reaction giving major products.
\[\begin{array}{cc}\ce{CH3 - CH = CH3 ->[Red P/Br2] A ->[Ag2O/H2O]B}\\|\phantom{.........................}\\
\ce{OH\phantom{.......................}}\end{array}\]
Advertisements
Solution
\[\begin{array}{cc}
\ce{3CH3-CH-CH3->[Red P/Br2][(Bromination)]3CH3-CH-CH3 +H3PO3->[Ag2O/H2O]3CH3-CH-CH3}\\
\phantom{}|\phantom{.............................}|\phantom{.....................................}|\phantom{}\\
\ce{\underset{2-Hydroxypropane}{OH}\phantom{................}\underset{2-Bromopropane(A)}{Br}\phantom{.........................}\underset{Propan-2-ol(B)}{OH}}
\end{array}\]
APPEARS IN
RELATED QUESTIONS
Complete the following reaction giving major products.
\[\ce{CH3 - CH = CH2 ->[HBr][peroxide] A ->[alc. KOH] B}\]
Complete the following reaction giving major products.
Name the reagent used to bring about the following conversion.
1-Chloropropane to 1-nitropropane
Arrange the following in the increasing order of boiling points.
- 1-Bromopropane
- 2- Bromopropane
- 1- Bromobutane
- 1-Bromo-2-methylpropane
Give reasons:
Haloarenes are less reactive than haloalkanes.
Convert the following:
tert-Butyl bromide to isobutyl bromide
Observe the following and answer the question given below.
Can it react by SN1 mechanism? Justify your answer.
Propane nitrile can be prepared by heating ____________
The following will react faster by SN1 mechanism
Explain. Aryl halides are less reactive than alkyl halides towards nucleophilic substitution reactions.
Explain the factors affecting SN1 and SN2 mechanism.
Nitroalkanes are obtained in laboratory from primary or secondary alkyl halides by the action of ______.
\[\ce{C6H5CH2Cl + KCN(alc) -> X + Y}\]
Compounds X and Y are ____________.
Which of the following carbocation is the most stable?
The SN2 reaction of a compound containing an asymmetric carbon atom always gives ____________.
Identify major product 'B' in the following reaction.
\[\ce{But-1-ene ->[HBr][Peroxide] A ->[AgCN][\Delta] B}\]
What is the major product obtained in the sulphonation of chlorobenzene with concentrated sulphuric acid?
The major product formed when 2-bromobutane is treated with alcoholic KOH is ______.
The order of reactivities of the following alkyl halides for an SN2 reaction is ______.
The compound that reacts the fastest with sodium methoxide is ______.
Explain the dehydrohalogenation reaction of 2-chlorobutane.
Complete the following reactions giving a major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{................}
\end{array}\]
Observe the following and answer the question given below:
Comment on the bond length of C-X bond in it.
Discuss β - elimination reaction.
Complete the following reaction sequences by writing the structural formulae of the organic compounds 'A', 'B' and 'C'.
\[\ce{2-Bromobutan ->[alc. KOH] A ->[][Br2] B ->[][NANH2] C}\]
Give a reason for the following:
Ethoxy ethane with conc. HI at 373 K gives C2H5OH and CH3I but not CH3OH and C2H5I.
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}\\
\end{array}\]
