Total: 2 points. 1 point for participation and 1 point for one or more correctly answered questions. PRINT YOUR NAME ON THE BACK ALSO. Draw the structure of the expected product per reaction. Circle syn or anti addition. 1. syn or anti 2. syn or anti H2SO4, H₂O no reaction CH3CH-CH2 H2SO4, HgSO4 H₂O но M syn 4. syn or anti 3. syn or anti 1. BH3, THF 2. H2O2, NaOH 1. OsO4 2. H₂O₂, H₂O 5. syn or anti Cl₂, H₂O 6. syn or anti Cl2, CH2Cl2 7. syn or anti 03. (CH3)2S 8. syn or anti MCPBA

Draw the full electron pushing mechanism for the reaction depicted including ALL intermediates (with lone pairs and formal charges). Clearly label the electrophile and nucleophile in each step where appropriate.

Draw the full electron pushing mechanism for the reaction depicted including ALL intermediates (with lone pairs and formal charges). Clearly label the electrophile and nucleophile in each step where appropriate.

This reaction is an example of conjugate addition of a nucleophile to an a,ẞ-unsaturated carbonyl. H3C LOCH3 H₂O H3C OCH3 OCH3 Draw the two resonance structures of the enolate anion intermediate for this reaction. • Draw an R1 group in place of CoA. The R group tool is located in the charges and lone pairs drop-down menu. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate resonance structures using the symbol from the drop-down menu. • O H CH3 ? [F