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A: we get Benzopinacol as product.
Predict the major organic product for this reaction.


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- H₂C + I H. H O AA common alkene starting material is shown below. Predict the major product for each reaction. Use a dash or wedge bond to indicate relative stereochemistry of substituents on asymmetric centers, where applicable. Ignore any inorganic byproducts Select to Draw Select to Draw 1. BH3-THF 1. Hg(OAc)2, Water 2. Н2О2, NaOН 2. NaBHa, NaОНHg(OAc)2 NaBH4, HO¯ TsCl, pyridine KCN CN CN (a) (b) CN OTs (b) (a) 2017 6-01-200 17C Haze AD 0 NG 1 rch hp
- Predict reagents needed to complete this E1 elimination reaction. BrYe P(ph)3 H i H O 2 CH₂CH₂OH H₂SO4 (catalytic)QUESTION 1 Complete the following synthetic transformation by selecung from the list of reagents below Each rangent te labeled with a letter. In the ancwer box, place the order of reagents using capital letters with no spaces. For example, if your synthesis involves using reagent A followed by B, and then C and then D, your answer would be: ABCD. BH3 A Br CrO3, Pyr B SECCEFLEED ? H₂O₂, NaOH с CrO3, Pyr D PCC
- N(CH3)2 Li, NH3, EtOHDIll. CI h) CI + CH;CH2OH i) HOUse the following reagent table for the reaction of : cyclohexanol + H2 SO4 → cyclohexene Chemical MW (g/mol) Density (g/mL) mmols used Amount used cyclohexanol 100.16 0.9624 1.50 mL Sulfuric Acid 98.08 1.83 1.0 mL cyclohexene 82.14 How many mmols of sulfuric acid are used? (answer with 2 decimal places, no units)

