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CHEM 210 EXAM BUNDLE(COMPLETE PACKAGE)Questions & Answers 100% Correct
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CHEM 210 EXAM BUNDLE(COMPLETE PACKAGE)Questions & Answers 100% CorrectCHEM 210 EXAM BUNDLE(COMPLETE PACKAGE)Questions & Answers 100% CorrectCHEM 210 EXAM BUNDLE(COMPLETE PACKAGE)Questions & Answers 100% CorrectCHEM 210 EXAM BUNDLE(COMPLETE PACKAGE)Questions & Answers 100% CorrectCHEM 210 EXAM BUNDLE(COMPLETE PACKAGE)Questions & Answers 100% Correct
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UMICH CHEM 210 - Exam #3 - Reaction Mechanisms 100% Correct.
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SN1 Reaction - ANSWER- Unimolecular nucleophilic substitution 
- 2 steps 
- Starting with enantiomerically pure product tends to result in some degree of racemization 
- Retention AND inversion at stereocenter (R and S) 
- 1 nucleophile is replaced by another nucleophile 
- Carbocation INTERMEDIATE forms 
- Rate is dependent only on substrate concentration 
 
1. LG leaves, forming a carbocation 
2. Nucleophile attacks the carbocation, forming the product 
 
SN2 Reaction - ANSWER- Bimolecular nuc...
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UMICH CHEM 210 - Exam #3 - Reaction Mechanisms 100% Correct
- Exam (elaborations) • 3 pages • 2024
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UMICH CHEM 210 - Exam #3 - Reaction Mechanisms 100% Correct 
 
 
SN1 Reaction - ANSWER- Unimolecular nucleophilic substitution 
- 2 steps 
- Starting with enantiomerically pure product tends to result in some degree of racemization 
- Retention AND inversion at stereocenter (R and S) 
- 1 nucleophile is replaced by another nucleophile 
- Carbocation INTERMEDIATE forms 
- Rate is dependent only on substrate concentration 
 
1. LG leaves, forming a carbocation 
2. Nucleophile attacks the carbocati...
-
UMICH CHEM 210 - Exam #3 - Reaction Mechanisms Accurate 100%
- Exam (elaborations) • 3 pages • 2024
- Available in package deal
-
- $10.49
- + learn more
SN1 Reaction - ANSWER- Unimolecular nucleophilic substitution 
- 2 steps 
- Starting with enantiomerically pure product tends to result in some degree of racemization 
- Retention AND inversion at stereocenter (R and S) 
- 1 nucleophile is replaced by another nucleophile 
- Carbocation INTERMEDIATE forms 
- Rate is dependent only on substrate concentration 
 
1. LG leaves, forming a carbocation 
2. Nucleophile attacks the carbocation, forming the product 
 
SN2 Reaction - ANSWER- Bimolecular nuc...
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