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- Which of the reactants are fastest at SN1 reaction mechanism? A B C DBromide Bhas normal activity (for a secondary bromide) towards SN1 substitution, but A has much higher reactivity and Chas much lower reactivity.Determine if CH3CH2ONa is a suitable reagent to deprotonate the following compound. Explain why. Draw the complete reaction, including the curved arrow mechanism.
- DRAW the product of the following reaction? Justify the stereochemistry...Draw the structure (including stereochemistry) of an alkyl chloride thatforms attached alkene as the exclusive E2 elimination product.Name attached compound and decide which stereoisomer will react faster inan E2 elimination reaction. Explain your choice.
- draw the oranic products formed in each reaction. can you answer c, d and fDraw the structure (including stereochemistry) of an alkyl chloride that forms each alkene as the exclusive E2 elimination product.Consider compound I below, which is structurally related to a natural product that was isolated from an extract of a Caribbean marine sponge (See J. Chem. Soc. 1994, 116, 6015). Answer the following questions about this compound (please explain answers) How many double bonds with E stereochemistry are present? _________ How many double bonds with Z stereochemistry are present? _________
- Draw the mechanism of the reaction shown. Will the product rotate plane polarized light? Breifly explain why or why not.I'm not understanding why there is a -oh group. Can you draw the stepwise mechanism so I can see why the leaving group is still thereWhen a carbonyl compound is attacked by a nucleophile resulting in the formation of a new stereogenic center, what product(s) will be formed? A) A racemic mixture of the two possible enantiomers B) Contains more of one enantiomer than another because of steric reasons around the carbonyl C) Contains more of one enantiomer than another depending on the temperature of the reaction D) Contains different products depending on the solvent used