| Sections | |||
|---|---|---|---|
| E2 Mechanism | 16 mins | 0 completed | Learn |
| Beta Hydrogen | 12 mins | 0 completed | Learn |
| E2 - Anti-Coplanar Requirement | 13 mins | 0 completed | Learn |
| E2 - Cumulative Practice | 8 mins | 0 completed | Learn Summary |
| E1 Reaction | 22 mins | 0 completed | Learn Summary |
| Solvents | 12 mins | 0 completed | Learn |
| Leaving Groups | 7 mins | 0 completed | Learn |
| Nucleophiles and Basicity | 6 mins | 0 completed | Learn |
| SN1 SN2 E1 E2 Chart (Big Daddy Flowchart) | 19 mins | 0 completed | Learn Summary |
| Cumulative Substitution/Elimination | 28 mins | 0 completed | Learn |
| Additional Practice |
|---|
| E2 - Anti-Coplanar Requiring Rotation |
| Rate Calculations |
| Substitution/Elimination Retrosynthesis |
| Intramolecular Substitution/Elimination Practice |
| The E1cb Mechanism |
Solution: Which of the following solvents can not be used with (CH3)3COK? a. (CH3CH2)2O b. (CH3)3COHc. H2O d. Liquid NH3 e. None of these
Problem
Which of the following solvents can not be used with (CH3)3COK?
a. (CH3CH2)2O
b. (CH3)3COH
c. H2O
d. Liquid NH3
e. None of these
Solution
(CH3)3COK is known as potassium t-butoxide which is a great bulky base used for E2 reactions. E2 reactions prefer
Practice Problems
In which of the solvents below would the reaction ...
Identify the correct potential energy diagram for ...
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Which conditions favor an efficient nucleophilic s...
Circle the only polar aprotic solvent:
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Circle “non-polar”, “polar aprotic”, or “polar pro...
What are the names and the structures of LDA, DMSO...
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What would be the effect of increasing solvent pol...
Rank the species below in order of increasing nucl...
Circle the strongest nucleophile in each category....
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In each of the pairs, determine the better nucleop...Which of the following solvents can not be used wi...Which of the following is a protic solvent?