Help!! 1. Draw the arrow pushing mechanism for the formation of tetraphenylcyclopentadienone. (6 pts) Ph Ph...
please help ans explain why: draw an arrow pushing mechanism to explain the formation of the products shown H2SO4 a. Br H3CO methanol b.
3. Draw a detailed arrow-pushing mechanism for the following transformation. (4 pts) Ph 1. NaNH2 Ph CI 2. H30+
3. Draw a detailed arrow-pushing mechanism for the following transformation. (4 pts) Ph 1. O3, CH2Cl2 요.. 2. CH SCH Ph H
". Draw a detailed arrow-pushing mechanism for the following transformation. (4 pts) Ph. Li(0) Ph Ph Ph NH30
3. Draw a detailed arrow-pushing mechanism for the following transformation. (4 pts) Ph 1. O3, CH2Cl2 2. CH3SCH3 om det. Vi
For the following electrophilic aromatic substitution: a.) draw complete arrow pushing mechanism for the movement of electrons to form product b.) draw arrow pushing for the formation of the electrophile c.) draw the major monoalkylated product Br. AlBr3
Draw a detailed arrow pushing mechanism for the following 1. Draw a detailed arrow pushing mechanism for the following: (5 pts) H2O, H2SO4 ОН но +
Draw the complete electron pushing arrow mechanism to show the formation of the final product shown. Explain every step of your mechanism. Explain why this is a product favored reaction. но*
For the reaction below: Draw the complete electron pushing arrow mechanism to show the formation of the final product shown. Explain every step of your mechanism. Explain why this is a product favored reaction. ii. H30* H20 OH A
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...