please help ans explain why: draw an arrow pushing mechanism to explain the formation of the...
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.
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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
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 +
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
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1. Draw the arrow pushing mechanism for the formation of tetraphenylcyclopentadienone. (6 pts) Ph Ph Ph Ph Ph I ,Ph heat Ph 2. Is the central ring of tetraphenylcyclopentadienone aromatic, non-aromatic, or anti-aromatic? 2 pts) 3. Why are two equivalents of base required to prepare the active thiamine catalyst? (3 pts)
Please draw the arrow pushing mechanism for the following reaction NO2 HNO3 + H2SO4
Draw the reaction mechanism for the formation of soap (with chemical structures and arrow pushing). ethyl acetate and 3M HCI, were used
Draw a detailed mechanism (that is, proper arrow pushing) for the formation of each compound, Analine to tribromoaniline, anisole to 2,4 dibromoanisole, acetanilide to bromoacetanilide
65. Draw the product of the following dehydration reaction. H2SO4 OH Ans: 68. Draw the mechanism for the following dehydration. LOH H2SO4 Ans: 71. Draw an energy diagram for the following reaction, assuming that it is exothermic. OH H2SO4 Ans: 73. What are the steps of arrow pushing involved in the following mechanism? ОН H2SO4 Ans:
Provide an arrow pushing mechanism she narrow pushing mechanism showing formation of the Trialkyl Borane product. 1.0 Equiv. BH3, THF Trialkyl Borane 3.0 Equiv. Has CHO Provide an arrow pushing mechanism showing why the trans isomer is the only product. HBr Major product