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- Drawing the SN1 and E1 Products in a ReactionDraw the SN1 and E1 products formed in the reaction of (CH3)3CBr with H2O.Rank the following from most reactive to least reactive in an SN1 reaction.Drawing the Oxidative Cleavage Products from an Alkene Draw the products when each alkene is treated with O3 followed by CH3SCH3.
- 4. Which arrow identifies the nucleophilic site in the molecule shown? <40 a dWhich substrate reacts with the cyanide anion ("CN) most rapidly in an SN2 reaction? O CH3CH,F O CH3CH2CH3 O CH3CH2OH O CH3CH2IThe given reaction scheme is an example of which type of reaction? O || R₁-C-OH + R₂-OH Oxidation Fischer esterification Nucleophilic substitution Reduction Rearrangement reaction Acid O || R₁-C-O-R₂ Meeting in "General"
- 1) Which substrate would react most rapidly in an SN2 reaction? O CH3CH2CH2CH=CHBr OCH2=CHCH2CH2CH2Br CH3CH2CH=CHCH2Br BrCH2CH2CH=CHCH3 OCH3CHBRCH=CHCH3The reaction of 3-methylhex-3-ene with HBr produces two stereoisomers. Draw the two-step mechanism, using good curved arrow notation. Identify the HOMO and LUMO in both steps and explain why two products are formed, along with the optical activity of the solution.Draw the product of the reaction of 1-methylcyclopentene with H30*/H20, as well as its preceding intermediate carbocation. H30* H20 intermediate product Why is the product you have drawn the only one that is observed? a) the heat of formation of this intermediate is lower b) the activation energy needed to form this intermediate is lower. c) the heat of formation of this product is lower d) the activation energy needed to form this product is lower
- If the anionic species shown were to eliminate a leaving group, the three possi- bilities would be H3C¯, CI, or CH30¯. Draw the curved arrow notation and the products for each of these elimination steps. Which is the major product? Why? CICurved arroows are used to illustrate the flow of electrons. Follow the arrows and draw the intermediate and product in this reaction. Include all lone pairs. Ignore stereochemistry. Ignore inorganic byproducts. : CH3OH2* но क protonation H3C CH3OH nucleophilic addition H. CH3 CHOH H-o H. e Type here to searchConsider the following reactants: CI OH Would elimination take place at a significant rate between these reactants? If you said elimination would take place, draw the major products in the upper drawing area. If you said elimination would take place, also draw the complete mechanism for one of the major products in the lower drawing area. If there is more than one major product, you may draw the mechanism that leads to any of them. Oyes Ono