Hello! The answer is D
A good note for these is when there are three elements, one being a singular element and another a compound and there’s a single switch, this could show a single-displacement
Have a good day gamer.
Answer:
See explanation below
Explanation:
You are not providing the starting material, however, I manage to find a similar question to this, so I'm gonna use it as a basis to help you answer yours.
Now let's analyze what is happening in the reaction so we can predict the final product.
We have a ketone here, reacting at first with LDA. This is a very strong base that is commonly used in reactions with ketones and aldehydes to promove a condensation. To do this, as LDA is a strong base it will occur firts an acid base reaction, substracting the most acidic hydrogen in the molecule (Which in this case, is the Beta hydrogen of the carbonile). This will cause an enolate formation.
Then, this enolate will react with the CH3I and form a new product. The final result would be a ketone with a methyl group now attached. In the picture 2, you have the mechanism and final product.
Hope this helps
The answer that h are looking for is c
All of the above because you didn't send us a image for reference..
The answer is C. Elastic potential energy