Cl + NH3 ethanol

Identify the nucleophile and leaving group and draw the products of attached substitution reaction.

+ In an SN2 reaction, a lone pair in the of the electrophile. A) a orbital; o orbital B) non-bonding orbital; o* orbital of the nucleophile reacts with the C) non-bonding orbital; o orbital D) TT orbital; σ orbital E) TT orbital; o* orbital

Determine which would be more reactive with a nucleophile

Determine whether the following reaction is an example of a nucleophilic substitution reaction: O" Molecule A + NO₂ Molecule B NO₂ + H

Please explain in detail idk how to go about this problem.

2. Draw a mechanism for the reaction of the nucleophile and the electrophile as indicated below. Also draw the product produced. CH3 H3C+CI CH3 + HO

This reaction does not correctly highlight the nucleophile because... + HCI A) In elimination reactions the alkene is always the electrophile B) In elimination reactions the alkene is always the nucleophile C) In electrophilic additions to alkenes the alkene is always the electrophile D) In electrophilic additions to alkenes the alkene is always the nucleophile

Which is/are NOT TRUE about bimolecular nucleophilic substitution reactions?  Select one or more: 1. A carbocation intermediate is formed. 2. A strong nucleophile displaces a halogen atom in a concerted mechanism. 3. Presence of polar aprotic solvents promotes this reaction. 4. Methyl halides react faster than secondary alkyl halides.

The reaction of an alkyl chloride with potassium iodide is generally carried out in acetone to maximize the amount of alkyl iodide that is formed. Why does the solvent increase the yield of alkyl iodide? (Hint: Potassium iodide is soluble in acetone, but potassium chloride is not.)