Advertisements
Advertisements
प्रश्न
How the following conversion can be carried out?
1-Bromopropane to 2-bromopropane
How is the following conversion carried out? Write reaction and condition only.
1-bromopropane to 2-bromopropane
Advertisements
उत्तर १
\[\ce{\underset{1-Bromopropane}{CH3CH2CH2Br} ->[Alc{.} KOH, \Delta][Dehydrohalogenation] \underset{Propene}{CH3CH = CH2} ->[HBr] \underset{2-bromopropane}{CH3 - CHBrCH3}}\]
उत्तर २
\[\begin{array}{cc}
\ce{\underset{1-Bromopropane}{CH3CH2CH2Br} ->[C2H5\overset{\ominus}{O}/KOH][\Delta] CH3CH = CH2 ->[HBr] CH3 - CH - CH3}\\
\phantom{...........................................................................}|\\
\phantom{.............................................................................}\ce{\underset{2-Bromopropane}{Br}}\\
\end{array}\]
APPEARS IN
संबंधित प्रश्न
Identify the product ‘D’ in the following sequence of reactions:
\[\ce{H3C - CH2 - CH2 - Cl \underset{KOH}{\overset{Alc}{->}} 'B' \overset{HBr}{->} 'C' \underset{Elther}{\overset{Na}{->}}'D'}\]
Predict all the alkenes that would be formed by dehydrohalogenation of the following halide with sodium ethoxide in ethanol and identify the major alkene:
2-Chloro-2-methylbutane
Write the structure of the major organic product in the following reaction:
\[\ce{(CH3)3CBr + KOH ->[ethanol][heat]}\]
How the following conversion can be carried out?
2-Chloropropane to 1-propanol
How the following conversion can be carried out?
2-Bromopropane to 1-bromopropane
Draw a neat, labelled energy profile diagram for SN1 reaction mechanism.
What are racemates?
Observe the following compounds and answer the questions given below.
(I)
\[\ce{\underset{\text{(II)}}{CH3 - CH2 - Br}}\]
- Identify the type of halides.
- Explain the nature of the C – Br bond in both of these halides.
- Which of these compounds will undergo aqueous alkaline hydrolysis readily? Write the reaction in support of your answer.
'A' is:
Deamination of meso- di bromobutane gives mainly:-
Identify the major product formed when 2-cyclohexylchloroethane undergoes a dehydrohalogenation reaction. Name the reagent which is used to carry out the reaction.
Elimination of bromine from 2-bromobutane results in the formation of ______.
The conversion of an alkyl halide into an alkene by alcoholic KOH is classified as ______.
A primary alkyl halide would prefer to undergo ______.
Which of the following alkyl halides will undergo SN1 reaction most readily?
An SN1 reaction at the asymmetric carbon of an enantiomerically pure chiral alkyl halide gives a product ______.
Major products A and B formed in the following reaction sequence are:
