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- Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?Provide the mechanism for the conversion shown below. CH3Li is effectively H3C-Li+. What type of mechanism is occuring?(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.
- Substitutions vs elimination. Pls help me identify the major products and the dominant mechanism. (SN1/SN2/E1/E2 or their combination)Under forcing conditions, sp2 CH bonds can be deprotonated, and sp2 chlorides can be eliminated. Draw two different mechanisms to account for the formation of the isomeric products C3H4 from the same chloride starting material.E 21 write mechanisms for the given reactions
- OCHEM... Give a detailed reaction mechanism for the reaction expected to occur when 2-bromo-2-methylpentane is heated with methanol. Draw clear structural formulas of all relevant species and use curved arrows to represent electron flow. Also, indicated which step is likely to be rate-determining.Identify which substitution mechanism best fits the following statement: The reaction proceeds through a concerted mechanism. A) SN1 B) SN2(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.(with explanation)
- I recovered 3 mL of water, how many grams of water was produced in the reaction please show how? Cyclohexanol can attack the carbocation intermediate formed during the synthesis of cyclohexene. Draw this side product with the molecular formula C12H22O.Explain the possible mechanism (Sn1/Sn2/E1/E2) given the reaction. Show the transfer of electrons/groups, and name the product.I need help to explain the mechanism below in steps in to words Preparation of Cyclohexanone by Hypochlorite Oxidation explain the mechanisms
