What type of stereochemistry is observed in the product of an E2 elimination reaction?
Practice Questions
1 question
Q1
What type of stereochemistry is observed in the product of an E2 elimination reaction?
R/S configuration
Cis/Trans isomerism
Z/E isomerism
Anti-periplanar arrangement
E2 elimination reactions require the leaving group and the hydrogen to be in an anti-periplanar arrangement, leading to the formation of the alkene.
Questions & Step-by-step Solutions
1 item
Q
Q: What type of stereochemistry is observed in the product of an E2 elimination reaction?
Solution: E2 elimination reactions require the leaving group and the hydrogen to be in an anti-periplanar arrangement, leading to the formation of the alkene.
Steps: 4
Step 1: Understand that an E2 elimination reaction involves the removal of a leaving group and a hydrogen atom from adjacent carbon atoms.
Step 2: Recognize that for the E2 reaction to occur, the leaving group and the hydrogen must be positioned in a specific way called 'anti-periplanar'.
Step 3: Know that 'anti-periplanar' means that the leaving group and the hydrogen are on opposite sides of the molecule, which helps in forming a double bond.
Step 4: Conclude that this arrangement leads to the formation of an alkene, which is a type of compound with a carbon-carbon double bond.
