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
Answer:
B
Explanation:
placenta comes after baby
The hydrogen and oxygen<span> atoms from H</span>₂O are <span>bonded together through covalent </span>bonding.
Addition of water to an alkyne gives a keto‑enol tautomer product and that is the product changed into 2-pentanone, then the alkyne need to had been 1-pentyne. 2-pentyne might have given a combination of 2- and 3-pentanone.
<h3>
What is the keto-enol means in tautomer?</h3>
They carries a carbonyl bond even as enol implies the presence of a double bond and a hydroxyl group. The keto-enol tautomerization equilibrium is depending on stabilization elements of each the keto tautomer and the enol tautomer.
- The enol that could provide 2-pentanone might had been pent-1- en - 2 -ol. Because an equilibrium favors the ketone so greatly, equilibrium isn't an excellent description.
- If the ketone have been handled with bromine, little response might be visible because the enol content material might be too low.
- If a catalyst have been delivered, NaOH for example, then formation of the enolate of pent-1-en - 2 - ol might shape and react with bromine.
- This might finally provide a bromoform product. Under acidic conditions, the enol might desire formation of the greater substituted enol constant with alkene stability.
Answer:10,0000 years
Explanation:
If it takes 2000 years to weather 1cm of limestone
It will take 5*2000 years to weather 5cm of limestone. This gives us 10000 years.