+ HO conc. H₂SO4 80° 2. CH3 H3C + CH3 H₂O a = Proton transfer b Lewis acid/base e = Electrophilic addition f = El Elimination c = Radical chain substitution g E2 Elimination d Radical chain addition CH3 CH3 = h Syl Nucleophilic substitution = i SN2 Nucleophilic substitution = j Electrophilic aromatic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -j for your answers.

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Q: Which one is sn1 or sn2 and state the mechanism?

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Q: 1. Predict the products of the folowing nucleophilic acyl substitution reactions. CHONa OCH, 2 pran

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Q: Br Br Br Me „Me Br Me Br Me Br Me Me A В D E F Ме Me Br Me Br Br Br Br -Br Me Me G H J K L

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A:

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Q: CH-CH, CHCI, Show the mechanism step by step to obtain the product

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Q: 2) When conjugated aldehydes or ketones are attacked by a nucleophile, often more than one product…

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Q: Predict the major product of electrophilic aromatic substitution.

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Q: Et CHCO₂H from starting material with no more than four carbon

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