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 proton which is easily abstracted in
1-Benzyl-3-propylbenzene is the proton which is present on carbon atom in between two phenyl rings, or the central carbon which is shared by two benzene rings.
This easy abstraction of proton is due to its high acidity. Remember those species are always more acidic whose
conjugate base is stable. Like the acidity of carboxylic acid is due to stability of the
acetate ion.
In our case the stability of conjugate base arises due to
stability of negative ion due to resonance. As shown below, the negative charge can delocalize on both rings.
I have shown the resonance of negative ion on both Phenyl rings with
Blue and
Pink colors.<span />
If a cell is placed in an isotonic solution, there will be no net flow of water into or out of the cell, and the cell's volume will remain stable. If the solute concentration outside the cell is the same as inside the cell, and the solutes cannot cross the membrane, then that solution is isotonic to the cell.
Hmm the answer is 2.454
No explanation needed it’s just 2.454
Answer:
6+9=15
mass number =15
mass number = no. protons + no. of neutrons
