5. (21 points - 7 points each) Mechanism Give an arrow pushing mechanism for the following...
2. (12 points, 6 points each) Give the arrow pushing mechanism for To of the following reactions. Draw the resonance structures of the intermediate. You MUST include the mechanism for the formation of the electrophile for electrophilic substitution reactions. Do not combine steps and be sure to show arrows and charges for all steps. Gie Twoyo.coc.c.m.m.ci.e groded..ay are wotcleurly marked hwiti only gade wor A. HNO, H,So B. 1. AICI 2. H2o C. OzN NO2 NaOCH2CH 02N. heat N/A D....
5(a). Predict the product for the following reaction. (b). Provide an arrow-pushing mechanism for the reaction above that accounts for the formation of the product. Explicitly include all non-bonding electrons and charges. Indicate whether each step is an initiation, chain propagation, or termination. (c). An additional product, shown below, is formed in the reaction from part (a). Provide an arrow-pushing mechanism that accounts for the formation of the additional product. (You may start from any intermediate from part (b))....
For the "mechanism" problems on this page, include intermediates and detailed "arrow Note: pushing" 16. Draw the mechanism for the following reaction, propagation steps only. (4 points) Br2 hv Br 17. Draw the mechanisms for the following reactions, using formal arrow pushing. Note: in some Vou would Ao wall to : hond ahangan.
4 (16 points - 8 points each Complete the following synthesis problems using the best synthetic route. Be sure to draw all the intermediate stap/products. Clearly mark the ones you would like graded. If not clearly marked, I will only grade the first problems X A Lon must ① - 75 aperone
Draw the arrow pushing mechanism for the following reaction. Clearly indicate arrows start and where they go in each step. Number each separate ey go in each step. Number each separate step in the mechanism and identify the pattern used in each step (10 points).
5. Show a complete arrow-pushing mechanism for the following reaction. (Triethylamine is a base. It may be helpful to label carbon atoms.) (3) H3Q Et3N, heat 0 Me Me 6. Show a complete arrow-pushing mechanism for the following reaction. (4)
Question 5 (37 pts.) Give a curved arrow pushing mechanism for the following reactions, and... 1) Show ALL important resonance contributors for all intermediates. 2) Add non-bonding electrons and C-H bonds to the line-angle structures as required. 3) Indicate the Lewis acid/.ewis base (LA, LB) at each step as appropriate, and whether they are also Bronsted acids/bases (LA/BA, LB,BB) 4) GIVE THE NUMBER OF STEPS IN YOUR MECHANISM H2O OH OH H.C-C-C-CHE CH, CH a) 10: CHỊ HẠC-C-C-CH - number...
Give a complete arrow-pushing mechanism for the following, indicate the Lewis and Bronsted acids/bases for each INTERMOLECULAR step only (LB, LB, BB, BA), but you do NOT need to show all resonance contributors for intermediates HCI (cat.) + H2O -ӧн
2. Draw a detailed arrow pushing mechanism for the following transformation (3 points): i 1)^_MGBT OH H2) H20
Question 8 (24 pts). For EACH, give a complete curved arrow pushing mechanism, and... 1) Show ALL important resonance contributors for all intermediates. 2) Add non-bonding electrons and C-H bonds to the line-angle structures as required 3) Indicate the Lewis acid/Lewis base (LA, LB) at each step as appropriate, and whether they are also Bronsted acids/bases (LA/BA, LB,BB) :Ö-MgBr Excess PhMgBr a) Ph Ph :Ö-MgBr O-H H3O+ b) Ph Ph Ph Ph part b) is not a trick, it is...