Asingle alkyl bromide reactant theoretically yields either of the given products, depending on the reaction conditions. draw the structure of the alkyl bromide compound.

Yields an ether either with one step reaction or may undergo a bimolecular reaction

Explanation:

Here the substitution reactions of alkyl halides: explores two mechanisms.

Step 1:

 The reaction takes place in a single step- direction, bond-breaking and bond-forming occur simultaneously this is a dissociative and produces carbonation. SN1 Reaction

Or

Step 2: bimolecular reaction and it is stereoselective. SN2

Note: As a rule, nucleophilic substitutions occur at sp3-hybridized carbons, and not where the leaving group is attached to an sp2-hybridized carbon.

Bonds on sp2-hybridized carbons are inherently shorter and stronger than bonds on sp3 - hybridized carbons, meaning that it is harder to break the C-X (Halide) bond in these substrates.

Where as SN2 reactions of this type are unlikely also because the (hypothetical) electrophilic carbon is protected from nucleophilic attack by electron density in the p bond.

SN1 reactions are highly unlikely, because the resulting carbocation intermediate, which would be sp-hybridized, would be very unstable .

So this above births the expression theoretical yield. Here is a question and the reactions.

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