Read the following road map carefully
The correct answer is option A
Both the ethers obtained by the two routes have opposite but equal optical rotation
One of the ether is obtained as a racemic mixture
Step II & III both are S2N reaction and both have inversion Step II has inversion but step III has retention
A compond A has the molecular formula C5H9CI. It does not react with bromine in crabon tetrachloride. On treatement with strong base it produces a single compound B. B shas a molecular formula C5H8 and reacts with bromine in carbon tetrachloride. ozonolysis of B produces a compound cC which has a molecular formula C5H8O2. Which of the following structures is that of A?
By the question (B) is correct answer.
Which of the following statement is correct
Product is :
Product is :
In the reaction The product is -
Example of pinacoi-pinacolone rearrangement
Given compound is in configuration due to walden inversion on attack by we get 'R' configuration
Example of pinacol pinacolone rearrangement.
The products of hydrolysis of
The product A is :
(CH3)3CCI + (CH3)3CO–K+ → Product
Stericaily hindered base leads to elimination product.
Neopentyl iodide is treated with aq. AgNO3 solution, a yellow precipitate is formed along with other compound which is
The major end product of the following reaction is
The major product P of the following reaction is
The product of following reacting is
Which can not be the product
The correct order of SN2 E2 ration for the % yield of product of the following halide is
(R) CH3 — CH2 — I
The correct answer is Option A
Least hindered halides give the fastest SN2 reaction as the hindrance increases. As the hindrance increases, the occurrence of SN2 reaction decreases.
The poduct in the given reaction is