Answer:
A. (CH3)3C-I reacts by SN1 mechanism whose rate is independent of nucleophile reactivity.
Explanation:
We must recall that (CH3)3C-I is a tertiary alkyl halide. Tertiary alkyl halides preferentially undergo substitution reaction via SN1 mechanism.
In SN1 mechanism, the rate of reaction depends solely on the concentration of the alkyl halide (unimolecular mechanism) and is independent of the concentration of the nucleophile. As a result of this, both Br^- and Cl^- react at the same rate.
Answer:
The chemical equation needs to be balanced so that it follows the law of conservation of mass.
Explanation:
Empirical evidence is information acquired by observation or experimentation
Answer:
Place 20.0 g NaOH(s) in a flask and dilute to 1.00 L with water.
Explanation:
