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
<span>subshells have two reasons of stability-
</span><span> 1) half filled and full filled subshells lead to symmetry as symmetry always increases stability in the nature.
</span>2)<span> in half filled and full filled subshells there are maximum no Of exchanges so exchanges releases energy so it increase stability.. Exchange of e-s also can b understood as delocalization of e-s which is similar like resonance and resonance always increases stability</span>
Answer:
Every single living thing are comprised of cells. Cells are the fundamental units of structure and capacity in living things. New cells are delivered from existing cells.
Answer:
A dono wat is da anser sori man hehe
#protactinium
- It lies in 7th period having Z=91
The outer electronic configuration is 6d^17s^2
- d-block element(transition)
So it will form polar covalent bond (2)
#Francium
Outer electronic configuration 7s^1
It will form ionic bond (3)