Advertisements
Advertisements
प्रश्न
Explain the mechanism of SN1 reaction by highlighting the stereochemistry behind it.
Advertisements
उत्तर

In SN1 reactions, if the alkyl halide is optically active, the product obtained in a racemic mixture. The intermolecular carbocation formed in slowest step being sp2 hybridized is planar species. Therefore the attack of the nucleophile OH on it, can occur from both the faces with equal case forming a mixture of two enantiomers. Thus SN1 reaction of optically active alkyl halides is accompanied by racemization.
APPEARS IN
संबंधित प्रश्न
The name of C2F4C12 is ______.
Which of the following reagent is helpful to differentiate ethylene dichloride and ethylidene chloride?
Consider the reaction,
\[\ce{CH3CH2CH2Br + NaCN → CH3CH2CH2CN + NaBr}\]
This reaction will be the fastest in
How will you prepare n propyl iodide from n-propyl bromide?
How does chlorobenzene react with sodium in the presence of ether? What is the name of the reaction?
Discuss the environmental effects of freons.
Explain the preparation of the following compound.
Chloroform
Explain the preparation of the following compound.
Freon-12
A hydrocarbon C3H6(A) reacts with HBr to form compound (B). Compound (B) reacts with aqueous potassium hydroxide to give (C) of molecular formula C3H6O. What are the (A), (B) and (C). Explain the reactions.
Two isomers (A) and (B) have the same molecular formula C2H4Cl2. Compound (A) reacts with aqueous KOH gives compound (C) of molecular formula C2H4O. Compound (B) reacts with aqueous KOH gives compound (D) of molecular formula C2H6O2. Identify (A), (B), (C) and (D).
