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:
none of the above
Explanation:
A system is said to have attained dynamic equilibrium when the forward and reverse reactions proceed at the same rate. That is;
Rate of forward reaction = Rate of reverse reaction
The implication of this is that the concentrations of reactants and products remain constant when dynamic equilibrium is attained in a system. This does not mean that the reactant and product concentrations become equal; it rather means that their concentrations do not significantly change once dynamic equilibrium has been attained.
Answer:
I think its a double reaction
Explanation:
WATER is wet to make it a more marketable commodity
