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- Give a detailed reaction mechanism for the reaction expected to occur when 2-bromo-2-methylpentane is heated with sodium methoxide. Draw clear structural formulas of all relevant species and use curved arrows to represent electron flow. Also indicate which step is likely to be rate-determining. The answer you sent before will be used for this question.Arrange the alkyl halides in order of increasing rate of solvolysis (slowest first)? I, II, III, IV IV, II, III, I II, III, I, IV III, II, I, IVWhich of the alkyl halides given below is faster with methoxide ion (-OCH3)SN2 gives a reaction, explain why and write down the reaction that occurs. 1-Bromopentane / 3-bromopentane
- (ii) The elimination reaction between 2-bromobutane and NaOCH2CH3 gives two organic products. Draw a mechanism for the reaction which produces the major organic elimination product and provide a rationale as to why that is the major product.Find the product formed by writing down the mechanism of the reaction.1) Predict the products (if any) that will be formed by the reaction below. If no reaction occurs, write NR after the reaction arrow. 2HClO4(aq)+ Co(s) =
- Write the reaction mechanism E2 between 2-bromopropane with sodium hydroxide, NaOH.This is the type of organic reaction wherein a single reactant splits into two products and is accompanied by the formation of a small molecule. addition substitution elimination condensation What is the name of the angle that a nucleophile approaches the carbon on the C=O bond? Borge-Dante Bürgi–Dunitz Baran-Daly Bunsen-DebyeFunctional groups such as alkynes react the same in complex molecules as they do in simpler structures. The following example of alkyne reaction were taken from syntheses carried out in the research group of E. J. Corey at Harvard University. You can assume that the reactions listed involve only the alkyne, not any of the functional groups present in the molecules. Draw the expected products for the following reaction .