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- What product(s) is(are) formed in the following reaction Br/CH-Clz Br plus enantiomer H3C Et Br Br H and H3C Br H3C Et Et Br он ...Et plus enantiomer H3C BrFor the reaction run at room temperature, compound I is formed. However, over prolonged reaction time, compound II becomes the major product. Which explains this phenomenon? H. но II O Compound Il is the both the thermodynamic and kinetic product. O Compound I is the kinetic product and compound II is the thermodynamic product. O Compound l is the thermodynamic product and compound Il is the kinetic product. O Compound l is the both the thermodynamic and kinetic product. O Both compounds I and II are the thermodynamic products. O Both compounds I and II are the kinetic products. %DRank the following according to INCREASING reactivity towards SN2: 1st (least reactive)? 2ND? 3RD? 4TH (most reactive)?
- Two products are formed when methylenecyclohexane reacts with NBS? Show how each is formed. Disregard stereoisomers.Consider the following arormatic.compounds N(CHh N(CH3)2 NH2 OCH, NON, NO NO2 OCH ARO MAT TIC HYD ROC a meto-substtuted compound Choose S the most reactive towards EAS the least reactive towards EAS Choose an ortho-substituted compoundWhat is the predicted product of the reaction shown? O & N(CH3)2 | IV (CH3)2NH H₂SO4 1. N(CH3)2 2. H3O+ || ОН HO |||
- 2-butanol reacts with HCl in the presence of ZnCl2 at high temperature. The final product of the reaction: A has inversion of configuration B is racemic C) none of these has retention of configurationWhich alkene is the most stable A В D A BWhich is true of a free energy diagram for an SN1 eaction? It shows one transition state. It always shows that the reaction is net exothermic. It never shows intermediates. It always shows that the reaction is net endothermic. It always includes multiple energy barriers.