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
from the following pair would undergo SN2 faster from the other?
a. CH3CH2CH2I b. CH3CH2CH2Cl
Complete the following reaction giving major products.
\[\ce{CH3 - CH = CH2 ->[HBr][peroxide] A ->[alc. KOH] B}\]
Complete the following reaction giving major products.
Give reasons:
Haloarenes are less reactive than haloalkanes.
Distinguish between SN1 and SN2 mechanism of substitution reaction.
Convert the following:
Propene to propan-1-ol
Convert the following:
2-Chloropropane to propan-1-ol
Complete the following reaction sequence by writing the structural formulae of the organic compound 'A', 'B' and 'C'.
\[\ce{2-Bromobutane->[Alc.KOH]A->[][Br2]B->[][NaNH2]C}\]
Observe the following and answer the question given below.
Name the type of halogen derivative.
Propane nitrile can be prepared by heating ____________
Major product of the following reaction is _______________
\[\ce{CH3-CH2-Mg-Br + NH3 ->?}\]
Nucleophilic substitution reaction of 2, 4-dinitrochlorobenzene is faster than p-nitrochlorobenzene. Give reason.
What is dehydrohalogenation? State the rule for the formation of the preferred product of dehydrohalogenation.
Ethyl bromide undergoes the following reaction:
\[\ce{\underset{Ethyl bromide}{C2H5Br} + \underset{(aq.)}{KOH} ->[\Delta] \underset{Ethyl alcohol}{C2H5OH} + KBr}\]
Which of the following is a WRONG statement?
Which of the following is least reactive towards nucleophilic addition?
\[\ce{C6H5CH2Cl + KCN(alc) -> X + Y}\]
Compounds X and Y are ____________.
Which of the following carbocation is the most stable?
When C2H5Br is treated with excess of alc. NH3, the major product obtained is ____________.
Write the product formed when alkyl halide reacts with silver nitrite.
Convert the following.
p-Nitrochlorobenzene to p-nitrophenol
The order of reactivities of the following alkyl halides for an SN2 reaction is ______.
The order of reactivity of the given haloalkanes towards nucleophiles is:
Which among the following statements is not correct about SN2 reaction mechanism?
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{...............}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl->[Na/dry ether]A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{...............}\\
\end{array}\]
Identify the chiral molecule from the following.
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{...............}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether]A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}
\end{array}\]
