(a)
Interpretation:
3-bromocylohexene or bromocyclohexane reacts faster in E2/E1 reaction is to be identified.
Concept Introduction:
An E1 reaction is a two-step reaction in which the
Major product is more stable
An E2 reaction is a concerted, one-step reaction in which the proton is the more stable alkene, unless the reactants are sterically hindered or the leaving group is poor.
(b)
Interpretation:
3-bromocylohexene or bromocyclohexane reacts faster in E2/E1 reaction is to be identified.
Concept Introduction:
An E1 reaction is a two-step reaction in which the alkyl halide dissociates forming a carbocation intermediate. Then a base removes a proton from adjacent carbon to a positively charged carbon.
Major product is more stable alkene.
An E2 reaction is a concerted, one-step reaction in which the proton is the more stable alkene, unless the reactants are sterically hindered or the leaving group is poor.
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CHEM 262 ORG CHEM EBOOK DIGITAL DELIVERY
- Which reacts faster in an E1 reaction?arrow_forwardDraw the product of each Robinson annulation from the given starting materials using −OH in H2O solution.arrow_forward2. Draw the products of each reaction. CH;CH2CI b. HNO3 Cl2 OCH3 Br -NO2 a. с. AICI3 H,SO4 FeCl3 3. Draw the products formed when each compound is treated with HNO3 and H2SO4. State whether the reaction occurs faster or slower than a similar reaction with be nzene.arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning