For the SN2 reaction, draw the major organic product and select the correct (R) or (S) designation around the stereocenter carbon in the organic substrate and organic product. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Η 1 D EN Select Draw Templates More C H D N Erase
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- Draw the organic product of the nucleophilic substitution reaction. Include all hydrogens atoms. CH3CH₂I + CH3CH₂O¯ → Select Draw Templates More //// C 0 H Erase Q2QSelect the correct IUPAC name for the following organic substrate, including the R or S designation where appropriate, and draw the major organic product(s) for the SN1 reaction. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Select Draw Rings More Erase HBr HO,Which statement is true concerning the two carbocations formed by the protonation (attachment of an H*) of 2-methylpropene? a) The activation energy associated with the primary carbocation intermediate is less than the activation energy associated with the tertiary carbocation. b) The rate of the formation of the tertiary carbocation is less (slower) than the rate of the formation of the primary carbocation. c) The activation energy and the rate of formation associated with the formation of the primary carbocation is greater. d) The activation energy is greater for the formation of the primary carbocation but its rate of formation is less. O a O b
- Consider this organic reaction Bri CHIỌ Draw the major products of the reaction in the drawing area below. If there won't be any major products, because this reaction won't happen at a significent s rate, check the box under the drawing area instead ZFill in the box with the major organic product of the following reaction mechanism. NaOH Draw the resonance structures of the product from the previous question. Draw in the curved arrow for the deprotonation of tert-butyl alcohol. to H K (metal) toDetermine which of the substrates will and will not react with NaOMeNaOMe in an SN2SN2 reaction to form an appreciable amount of product. Answer Bank (CH3)2CHBr(CH3)2CHBr (CH3)3CBr(CH3)3CBr CH3CH2CH2BrCH3CH2CH2Br CH3CH2CH2OHCH3CH2CH2OH (CH3)3CCH2Br(CH3)3CCH2Br CH3CH2CH2NH2CH3CH2CH2NH2
- Consider the mechanism of the reaction shown below. Give the structure of the next important organic reaction intermediate along the reaction coordinate. Your answer could be the final product. H. -? HBr Edit Click on the drawing box above to activate the MarvinSketch drawing tool and then draw your answer to this question. If there is no reaction, then check the "no reaction" box below. no reactionOf the two unimolecular reactions shown, decide which you think would be faster, i.e., which would have a higher relative rate constant (krel). Based on your answer, draw two lines on one reaction coordinate diagram that show the relative progress of each reaction along its path to product indicated. Bond dissociation energy of the C-LG bond. Nature of the leaving group (LG). The relative size of activation energy (Ea) for each reaction Hammond's postulate. Relative thermodynamic stability of the reactive intermediates. Influence of the solvent (if given) on the reactions and intermediates.Draw the structure of the missing reactants, intermediates, or products in the following mechanism. Include all lone pairs except on metal atoms. Ignore stereochemistry. Ignore inorganic byproducts. OAc OAc Edit MercurinÂum Intermediate
- Draw the structures of the missing reactants, intermediates, or products, in the following mechanism. Use wedges and dashes to indicate stereochemistry when appropriate.Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction.please answer both, thank u!