What is the stereochemical configuration of the product formed from the reaction of (R)-2-bromobutane with a strong nucleophile in an SN2 reaction?
Practice Questions
1 question
Q1
What is the stereochemical configuration of the product formed from the reaction of (R)-2-bromobutane with a strong nucleophile in an SN2 reaction?
R
S
R and S
Neither R nor S
The SN2 reaction will invert the configuration of (R)-2-bromobutane, resulting in the (S) configuration.
Questions & Step-by-step Solutions
1 item
Q
Q: What is the stereochemical configuration of the product formed from the reaction of (R)-2-bromobutane with a strong nucleophile in an SN2 reaction?
Solution: The SN2 reaction will invert the configuration of (R)-2-bromobutane, resulting in the (S) configuration.
Steps: 5
Step 1: Identify the starting material, which is (R)-2-bromobutane. This molecule has a specific 3D arrangement of atoms.
Step 2: Understand that an SN2 reaction involves a strong nucleophile attacking the carbon atom that is bonded to the bromine atom.
Step 3: Recognize that during the SN2 reaction, the nucleophile will attack from the opposite side of the leaving group (bromine), leading to a change in the configuration.
Step 4: Since the starting material is (R)-2-bromobutane, the attack from the nucleophile will cause the configuration to invert.
Step 5: Conclude that the product formed will have the (S) configuration due to this inversion.
