Answer:
an increase in 1-butene was observed when t-butoxide was used
Explanation:
When a base reacts with an alkyl halide, an elimination product is formed. This reaction is an E2 reaction.
Here we are to compare the reaction of two different bases with one substrate; 2-bromobutane. Both reactions occur by the E2 mechanism but follow different transition states due to the size of the base.
The Saytzeff product, 2-butene, is obtained when the methoxide is used while the non Saytzeff product, 1-butene, is obtained when t-butoxide is used.
The Saytzeff rule is reliable in predicting the major products of simple elimination reactions of alkyl halides given the fact that a small/strong bases is used for the elimination reaction. Therefore hydroxide, methoxide and ethoxide bases give similar results for the same alkyl halide substrate. Bulky bases such as tert-butoxide tend to yield a higher percentage of the non Saytzeff product and this is usually attributed to steric hindrance.
The trough and the hill part
Answer:
The correct answer is "True".
Explanation:
A reaction mechanism is a theoretical postulate that tries to explain in a logical way which are the elemental and intermediary reactions that happen in a chemical reaction and that allow to explain the qualitative and quantitative characteristics observed in its development, in which a unique molecular event is described in each elemental step.
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Its chemical name is Aluminium Sulfite.
I think the answer is ( A and C ) why I picked a and c it’s because a and c look the same answer. I hope it helped you
