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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?Azo coupling reaction. Provide a mechanism with intermediates and arrowsUnder 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.
- A carbocation intermediate is central to which of these reaction types? E1, E2, SN1, SN2 ? Choose 1Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- ΔH=-75 kJ/mol Rate = k [CH3CH2Br][CH3COO-] Which reaction energy profile would be the best representative of the data provided?In the formal SN1 mechanism, the reaction has two steps; however, in reality ____________ steps are actually needed to produce the final product. 3 5 2 4 1
- Identify which substitution mechanism best fits the following statement: The reaction proceeds through a concerted mechanism. A) SN1 B) SN2Explain the possible mechanism (Sn1/Sn2/E1/E2) given the reaction. Show the transfer of electrons/groups, and name the product.Substitutions vs elimination. Pls help me identify the major products and the dominant mechanism. (SN1/SN2/E1/E2 or their combination)
- provide a detailed mechanism for the dehalogenation of meso-1,2 dibromo 1,2 diphenyl ethane. show all electron movements + use arrows. Include intermediates.What are the relevant transition states for this reaction?what is the expected major product of HBr addition to the alkene shown below? Show the mechanism