Provide a synthetic route to the following compound(s) а. Br он from "H b. from SCH3

Which of the aromatic compounds shown in Image 1 reacts faster than benzene in electrophilic aromatic bromination? A. B. C. D.

Organic Christry The resulting the reaction

17. Provide the major product of the following reaction. If no reaction occurs, write "n.r." SO₂H Cl₂ AICI (if o,p-substituted products are possible, only provide the major para-substituted product, otherwise, only provide the meta-substituted product)

Which reaction intermediate (A or B) is more likely to form in the epoxide ring opening reaction? Reactions prefer to react through lower energy intermediates. Hint: how might you justify one structure being lower in energy than the other? Draw structures as part of your explanation why. Structure A Structure B ерoxide ring opening HO, : ОН Which alcohol structure shown below would be less acidic? Explain why. F F. Br Br Br

Which of A to E correctly shows the structure of the major organic product obtained from the ozonolysis reaction shown below?

7. Supply the missing reagents for the reactions shown CI CI

HW.pdf oads/CH8%20HW.pdf 2 / 4 90% 3. Provide reagents for each of the following transformations: ... OH +

Provide a plausible arrow pushing mechanism for the reaction below. 1 eq. H20 MEOH Но. OMe cat. H-A OH