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- Predict the product for the following Sn2 reactions.Complete the three following SN1 reactions by drawing the structure of the major product(s). If the product is a mixture of stereoisomers, draw all possibilities and indicate their relationship (i.e. enantiomers or diastereomers).The following reaction has a ΔSsystem < 0 O2(g) → 2O(g) T or F can you explain why this is false?
- Optically active butan-2-ol racemizes in dilute acid. Propose a mechanism for this racemization.How does the rate of an SN2 reaction change as the alkyl group in the substrate alkyl halide changes from CH3 1° 2° 3°?Draw the products of the SN1 reaction below and use wedge-and-dash bonds to indicate the stereochemistry of any stereogenic centers.
- Propose a mechanism for this example of a pinacol rearrangemenWhich of the following ff. halides is most likely to react through the SN1 mechanism? i. CH3Clii. CH2=CHCH2CH2Cliii. CH3CH=CHCH2Cl iv. CH2=CHCl5. Predict the product and show the mechanism of the following reaction:(Write out complete equations showing the structure of all reactants and products.) 2-methoxyheptane + Excess conc HBr/heat ----->