Answer:
See explanation
Explanation:
The first step in this reaction is a unimolecular reaction. It involves the formation of the carbocation. This is so because tertiary alkyl halides only undergo substitution by SN1 mechanism due to sterric crowding.
The second step in the reaction is bi molecular. In this step, the carbocation now combines with the OH^- to yield the alcohol.
Net equation of the reaction is;
(CH3)3CBr + OH^- -------> (CH3)3COH + Br^-
The intermediate here is the carbocation, (CH3)3C^+
B. 1500m + 180m = 1680m and is the greatest
Answer:
See below ↓↓↓
Explanation:
Helminths = 1 Most Difficult
Fungi = 2 Moderately Difficult [Option not given, but 2 is right answer]
Bacteria = 3 Least Difficult
Answer:
Explanation:
The principle applied is the Markovnikoff's rule which states that when hydrogen chloride adds to a double bond, the hydrogen atoms join to the carbon that already has the most hydrogen atoms bonded to it. The rule wa postulated by a russian chemist known as Vladimir Markovnikoff.
In the markovnikoff's rule, there are sveral conditions that must be met, one of them is that no free radicals must be involved.
The reaction and the structure of the product is as shown in the attachment.