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Stack #4544534

QuestionAnswer
Tertiary Alkyl Halides Strong base (like alkoxide) E2 reaction
Tertiary Alkyl Halides Weak nucleophile (like water) SN1 reaction (E1 is minor unless highly substituted alkene forms)
Tertiary Alkyl Halides SN2 possibility SN2 not possible with tertiary halide
Secondary Alkyl Halides Strong base (like alkoxide) E2 reaction
Secondary Alkyl Halides Strong nucleophile (like sodium azide) SN2 reaction
Secondary Alkyl Halides Weak nucleophile (like water) SN1 reaction (E1 minor)
Primary Alkyl Halides Strong nucleophile or strong base (like sodium azide or alkoxide) SN2 reaction (E2 less likely)
Methyl Halides Strong nucleophile or strong base (like sodium azide or alkoxide) SN2 reaction
Tertiary Alcohols H₂SO₄ E1 reaction
Tertiary Alcohols HX SN1 reaction
Secondary Alcohols H₂SO₄ E1 reaction
Secondary Alcohols HX SN1 reaction (may proceed SN2 in select cases)
Primary Alcohols H₂SO₄ Pseudo-E1 via rearrangement to form carbocation (except ethanol)
Primary Alcohols HX SN2 reaction (SN1 via rearrangement less likely)
Ethanol H₂SO₄ E2 reaction
Ethanol HX SN2 reaction
Methanol HX SN2 reaction only (no elimination possible only one carbon atom)
Created by: user-1992814
 

 



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