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- Rank the following nucleophiles in order from slowest SN2 reaction rate to fastest if DMSO is the solvent. ОН PH SH A B D EList the following in increasing order of nucleophilic strength. CH3COO-, H2O, CH3O-, OH-, CH3CH20-Rank the nucleophiles in following group in order of increasing nucleophilicity. −OH, Br−, F− (polar aprotic solvent)
- The nucleophile approaches from the opposite side of the carbon with the leaving group in which reaction mechanism? O E2 O SN1 O SN2 O SN1 and SN2Which compound is most nucleophilic? * О Option 5 О снзSH CH3SH О снзон О снзсо2н CH3CO2H О 120 Н20Identify the strongest nucleophile. HO™ O NaSH OCH3CH₂OCH2CH3 Or
- For each reaction below identify the electrophile and the nucleophile.Br CH₂O-¹ Na+¹ CH₂OH Classification of Reactant: 1° RX 2° RX 3ºRX H₂CO-¹ (circle one): Strong basic nucleophile Weak basic nucleophile Reaction Type (circle one): E1 E2 S1 S2 Electrophilic Addition Radical Addition If Addition (circle any applicable): Markovnikov Anti-Markovnikov Anti Addn Syn AddnWhich nucleophile would prefer simple addition over conjugate addition? CH3MgBr NaCN CH3CH2NH2 (CH3CH2)2CuLi