(c) What is the solvent effect on the SN1 and SN2 reactions?', (d) Which reactant in each of the following pairs is more nucleophilic? Explain. (i) -NH2 and NH3 (ii) I'and CI
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A: Detail mathematical calculation to find out the volume of CO2 is shown below
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Solved in 3 steps with 2 images
- Which of the following compounds (A or M) would be the better choice for a nucleophilic substitution reactionusing Compound T as the starting material and DMSO as the solvent? Would the resulting reaction be SN1 or SN2?How does bromobenzene react differently from benzyl chloride under SN1 and SN2 conditions, and why?Explain the Summary of Alkyl Halides and SN1, SN2, E1, and E2 Mechanisms ?
- When drawing organic chemistry mechanisms with NaOCH3, do we automatically dissociate it into Na+ and OCH3-, making it easier to go through SN2 and/or E2 reactions? Does NaOCH3 dissociate, and is this why it is a strong nucleophile?what would a detailed step-by-step mechanism be for a reaction between bromine and trans-stilbene if the solvent, ethanol, is a stronger nucleophile than the bromide ions?Arrange the structure on the image with regard to the reactivity towards nucleophilic acyl substitution 1 being the least and 3 being the most
- Understanding different substitution and elimination pathways gives useful insight into chemical mechanisms and pathways. Give the different important aspects of the Sn1, Sn2, E1, E2, and E2cB reactions.The reaction proceeds by an SN2 mechanism. Draw a sketch of the structure of the transitionstate, clearly indicating:- the geometry at the electrophilic carbon centre, and- bonds in the process of being broken or formed with dotted lines, if present.Working Backwards Parte Deux. a.First, identify which functional groups changed during the reaction. Did stereochemistry change too? b. Based on your answers to A and B, what kind of reaction occurred here, SN1 or SN2? c.Suggest reagents and solvent that could accomplish this reaction.