Question 5 Describe the mechanism of the following reaction and replace the R groups with groups from the given list: R₁ R3- OR3 OR5 10 Base + R6-OH 13 R2 OR4 11 12 R4 Your selection of R groups for the products must be consistent with those in the substrates.
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- 7B What is the product of the following cleavage reaction and what is its stereochemistry? Me H Br H NaOEtfor each reaction give the expected substitution product and predict wether the mechanism will be first order (SN1) or second order (SN2) a) 2-chloro-2-methylbutane + CH3COOH b) isobutyl bromide + NaOMe c) 1-iodo-methylcyclohexane + CH3CH2OHState the mechanism of the following reactions (NOTE: draw theproper settings where applicable)
- The reaction of sodium borohydride with ketones proceeds rapidly at room temperature, forming an intermediate borate ester which is hydrolyzed to give the product alcohol: 4 R2C=O + Na+BH4- ---> (R2CHO)4B-Na+ (R2CHO)4B-Na+ + 2H2O ---> 4R2CHOH + Na+BO2- Rewrite these two steps using benzil as the ketone, and using structural formulas throughout, rather than the condensed forms above.Give the organic product formed in each of the following reactions, draw a 3-D representation for the product molecule showing the correct configurationSuggest the mechanism for the following reaction