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- 6. Circle the structure with the most nucleophilic double bond. Put a box around the structure with the least nucleophilic double bond. OH L I X6. Place an "X" in the box below the nucleophile that will react the most quickly with methyl iodide. Place an "O" in the box below the nucleophile that will react the most slowly with methyl iodide.Consider this nucleophilic substitution reaction. 1. Highlight the electrophilic carbon in red, and highlight the leaving group in blue. Highlight the atom in the nucleophile that will attack the electrophilic center in green. Only atoms need to be highlighted and not the lone pairs or formal charges. 2. Draw the product(s) of the reaction. Include all lone pairs.
- How might nucleophilic catalysis work?Draw out a possible mechanism.For each reaction, write the letter corresponding to the type of reaction (before the number) and draw the MAJOR product (in the product side). A. Nucleophilic Addition B. Nucleophilic Condensation C. Nucleophilic Acyl Substitution"Nucleophilic substitution reaction"" When does the bond between the leaving group and C break? Does it break at the same time that the new bond between the nucleophile and C forms? Or Does the bond to the leaving group break first.
- Draw the product of nucleophilic substitution with attached neutral nucleophile. When the initial substitution product can lose a proton to form a neutral product, draw the product after proton transfer.4. Circle the molecule that would react fastest in an SN2 reaction. In addition, classify cach molecule as methyl, 1°, 2° or 3°. CI CICircle all molecules that contain acetals.