Draw a reasonable arrow-pushing mechanism for the transformation shown. Please be certain to adhere to the guidelines laid out in the announcement. H CI CI HCI (xs)
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- Provide an arrow pushing mechanism for the following transformation and clearly circle the slowest (rate-determining) step in the mechanism.Draw the product of this reaction and states its IUPAC name, and states what type of mechanism is occuring (eg. SN1, SN2, E1, E2, etc)?Draw the structure (including stereochemistry) of an alkyl chloride thatforms attached alkene as the exclusive E2 elimination product.
- Provide the reagent necessary and mechanism for the transformation below (more than one step is required). Additionally provide the IUPAC name for the starting materialPropose an efficient synthesis for each of the ff transformationIn each case below select the synthetic procedure that could be used to carry out the transformation shown
- Provide the neccessary reagents next to the arrowsBromide Bhas normal activity (for a secondary bromide) towards SN1 substitution, but A has much higher reactivity and Chas much lower reactivity.Consider the following reaction scheme: (i) Provide the reagent(s) required for this transformation. (ii) Draw a curved arrow mechanism and comment on the stereoselectivity.