What is the product obtained when $trans-2-phenyl-1-bromocyclopentane$ is treated with alcoholic $KOH$?
- A$4-phenylcyclopentene$
- B$2-phenylcyclopentene$
- C$1-phenylcyclopentene$
- D$3-phenylcyclopentene$
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Similar Questions
An alkyl halide $X$ $(C_4H_9Br)$ undergoes nucleophilic substitution by $S_N2$ reaction. The product of $X$ on reaction with $Mg/\text{dry ether}$ followed by $D_2O$ is:
Which reagent is used to convert an $Alkyl \ halide$ $(R-X)$ into an $Alkyl \ nitrite$ $(R-O-N=O)$?
$CH_3-CH_2-CH(Br)-CH_3 \xrightarrow{Alc. KOH} X$ (major)
$CH_3-CH_2-CH(NMe_3^+) - CH_3 \xrightarrow{EtONa, \Delta} Y$ (major)
Product $(X)$ and $(Y)$ respectively are:
$CH_3-CH_2-CH(NMe_3^+) - CH_3 \xrightarrow{EtONa, \Delta} Y$ (major)
Product $(X)$ and $(Y)$ respectively are:
Medium
View SolutionWhat is the correct order of $C-X$ bond strength in $CH_{3}X$?
What is the major product obtained in the reaction of $1-$phenyl$-2-$bromobutane with $NaOMe$?
Medium
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