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- Draw the mechanism fot his reaction. B = [IrCl(CO)(PPH3)2]Predict the products of each reaction. If the product has stereochemistry, draw the products using dash wedge notation. Draw all stereoisomers formed and indicate if the product is achiral or chiral. Draw a mechanism for each reaction clearly showing how the product stereochemistry is produced. You are not required to draw the final step(s) in the mechanism for reactions involving organometallic intermediates.SN1 and El reactions both proceed through carbanion intermediates A) True B) False
- Predict the products of each reaction. If the product has stereochemistry, draw the products using dash wedge notation. Draw all stereoisomers formed and indicate if the product is achiral or chiral. Draw a mechanism for each reaction clearly showing how the product stereochemistry is produced. You are not required to draw the final step(s) in the mechanism for reactions involving organometallic intermediates.What is a key difference between the following two reactions? a) CH3MgBr would deprotonate the alpha position and CH3NH2 would add directly to the C=O b) CH3MgBr would deprotonate the alpha position and CH3NH2 would add in the beta position c) CH3MgBr would add directly to the C=O and CH3NH2 would add in the beta position d) CH3MgBr would add in the beta position and CH3NH2 would add directly to the C=ORank thr stability of the following sets of reaction intermediates.