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What is the effect of a protic solvent in an SN1 reaction?
Step by step
Solved in 2 steps
- What direction does the nucleophile approach the substrate in an SN2 reaction?Define the difference between E1 and E2 mechanisms ?Which of the following Phase 2 reactions is likely to target a N-bearing functional group specifically? a Acetylation b Glycine conjugation c Glucuronic acid conjugation d Sulfation
- A) Describe substrate structure and condition that favor SN1 reactions taking place over SN2. B) What conditions promote E2 reactions.Which of the following substituent is a meta-directing deactivator? a amino group b halogenation group c phenyl group d carboxyl groupWhich of the following substituent is an ortho/para-directing deactivator? a amino group b halogen group c phenyl group d carboxyl group
- how the r-group affects the elimination, specifically E-1 reaction and how a different r-group would have a different effectplease explain why this happends, im having trouble in this section. Part A Chymotrypsin, an enzyme that hydrolyzes peptide bonds in proteins, functions in the small intestine at an optimum pH of 7.7 to 8.0. How is the rate of the chymotrypsin-catalyzed reaction affected by each of the following conditions?Which factor will promote an Sn1 reaction?1. Strong base 2. nonpolar aprotic solvent 3. 1 degree substrate 4. good leaving group