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- 1. Propose the complete reaction mechanism and reagents used for the production of hexan-2-olfrom hex-1-ene. Name the reagents, intermediate and final product/s formed.4.35 Assuming that the rate-determining step in the reaction of 1-hexanol with hydrogen bromideto give 1-bromohexane is an attack by a nucleophile on an alkyloxonium ion, write an equationfor this step. Use curved arrows to show the flow of electrons.QUESTION 7 Identify the best nucleophile in a substitution reaction at a primary carbon. a. H2O b. (CH3)3CO- c. CH3CH2O- d. HO-
- 2-butanol + NOx + hv (assume the carbon-hydrogen bond on the carbon adjacent to the carbonwith the alcohol group is the weakest) For each mechanism, provide the photolytic cycle, a source for hydroxyl radical (if needed) AND atermination step. You may stop when you have accounted for all radicals AND all VOCs are stable (i.e., ifformaldehyde is a product of your mechanism, you do not have to oxidize that molecule to).find a synthesis for each one given below. reaction mechanism is not necessary a) acetylene ---> 2-bromopentane c) ethyl bromide --->trans-3-hexane e) gasoline alcohol ---> benzaldehyde7. Complete the following reaction and propose a mechanism.