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what does the complete SN2 mechanism (with curved arrows) of the reaction of 2-bromobutane with an
iodide ion look like?
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- Provide the full mechanism of this SN2 reaction.The following is a nucleophilic substitution reaction of R-3-chloro-2-methylhexane with "OCH3. The optical rotation of the solution after the reaction was complete was +11.4° CH3 Н. H3C. CH3 "OCH, H2 H. The mechanism for this reaction is SN2 Draw the organic molecule(s) which is(are) formed in this reaction. Do not include molecules like H,O or HCl. Draw the specific configuration (R or S) at any chiral carbons within your product(s). If both configurations are formed in the product(s), draw both as separate molecules/products.Draw the mechanism from the reactants to the product shown in the picture. What role do the nitro groups play electronically? Why would the reaction be much slower if these nitro groups weren’t attached to those benzene carbons? Draw structures to support answer
- In an E2 mediated elimination reaction of an alkyl halide (H-X) using NaOCH3 as base, which of the following statement is not true? O The reactivity order for alkyl halides (RX) is tertiary secondary> primary. O The rate of reaction = k2 (alkyl halide] [NaOCH₂] O The reaction occurs in a single step. O The rate is independent of the leaving group.For this mechanism, how come the iodine doesn't attach to a carbocation on the right (with the two methyl groups coming off of it)? Is it because TsO is a better leaving group? If so, why is this?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?
- Is NaOCH2CH3 also a strong nucleophile? if so and Br wasn't a 3 degree alkyl halide, would it also undergo an Sn2 reaction? what would the major product be then?Draw the product of the following nucleophilic substitution reaction and provide a full mechanism for its formation. Na* NH-CH; Chlorobenzene CH3NH2Give a complete mechanism for the ionic addition of HBr to 1-methylcyclopentene.
