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.
The standard atomic weight is the average mass of an element in atomic mass units ("amu"). Though individual atoms always have an integer number of atomic mass units, the atomic mass on the periodic table is stated as a decimal number because it is an average of the various isotopes of an element.
The last answer
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Answer:
N,N-dimethylacetamide is formed.
Explanation:
- It is an example of a nucleophilic addition-elimination reaction. Here dimethylamine acts as a nucleophile.
- In the first step, dimethyl amine gives nucleophilic addition reaction at carbonyl center of acetyl chloride.
- In the second step, removal of Cl atoms occurs.
- In the third step, deprotonation takes place from amino group to produce N,N-dimethylacetamide.
- Full reaction mechanism has been shown below.
