Answer:
=0.00123
Explanation:
Look at the attachments below
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Primary alkyl halides tend to undergo the SN2 reaction mechanism in nucleophilic substitution since there is less steric hindrance for nucleophilic attack and the carbocations that they form are not as stable as those formed from tertiary alkyl halides.
1-bromopentane > 1-bromo 2-methylbutane > <span>1-bromo-3-methylbutane</span>> 2-bromo 2-methylbutane
Answer:
3
Explanation:
pH=-log(H+)
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Because the nuclear charge increases across a period and so it has a stronger pull on the outer electrons and will pull in the radius
Answer:
lighting a match is the answer.