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9 Cards in this Set
- Front
- Back
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Methyl halides react with sodium ethoxide in ethanol only by this mechanism
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SN2
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Unhindered primary halides react with sodium ethoxide in ethanol mainly by this mechanism
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SN2
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When cyclohexyl bromide is treated with sodium ethoxide in ethanol, the major product is formed by this mechanism
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E2
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The substitution product obtained by solvolysis of tert-butyl bromide arrises by this mechanism
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SN1
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In ethanol that contains sodium ethoxide, tert-butyl bromide reacts mainly by this mechanism
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E2
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These reaction mechanisms represent concerted processes
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SN2 and E2
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Reactions proceeding by this mechanism are stereospecific
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SN2 and E2
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These reaction mechanisms involve carbocation intermediates
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SN1 and E1
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These reaction mechanisms are the ones most likely to have been involved when the products are found to have a different carbon skeleton than the substrate
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SN1 and E1
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