Question

I Select ] I Select ] True False I Select J ▼ The identity of the nucleophile affects the rate of an SN1 reaction SN2 reactions proceed via frontside attack ▼ Bimolecular reactions tend to be stereoselective. Select ] SN2 reactions invert all stereocenters in a haloalkane Select] Cl-, OH-, and H- are good all leaving groups [ Select ] Good bases tend to be good nucleophiles Select ▼ Branching adjacent to a reacting carbon slows SN2 reactions due to steric hindrance [ Select ] SN1 reactions are slowed by hyperconjugation of the carbocation intermediate Select] The rate determining step for SN1 reactions is the same as the rate determining step for E1 reactions [ Select ] It is possible to get E1 alone but SN1 is always accompanied by E1. Select] Leaving group ability depends only on pKa of the conjugate acid [ Select ] ▼ Good nuclephiles are also good leaving groups Select ] ▼ Protic solvents solvate large ions better than small ions because of increased surface area

Answer 1

falsey because nucleophile is not involved in sate determining step in SA seaction bol false, SN, reactions proceedia - Backside attacks True SNL & E₂ both biomolecular - reactions are stereoselective Las in both one stereoisomer product L is formed selectively over thee false, No it only inverts the sterecenter that is being attacked other sterexenter retains itd stessochemistry False ha oh is a poor leaving group & H is a extemely post leaving group as oll- is a conjugate base of Ho & H is a conjugate base of H₂ a they are for adds True. A good base is usually a good nucliophile T except those which are sterically 6 Scanda hündered Cansarner

z Torue because addition of substitutes on neighbouring carbon sloo nudleophile substion I will C adeachish CamScanner.