Answer:
Potassium (K) and Lithium (Li) for the fist one i cant see the second
Explanation:
Answer:
\frac{dh}{dt}_{h=2cm} =\frac{40}{9\pi}\frac{cm}{2}
Explanation:
Hello,
The suitable differential equation for this case is:

As we're looking for the change in height with respect to the time, we need a relationship to achieve such as:

Of course,
.
Now, since the volume of a cone is
and the ratio
or
, the volume becomes:

We proceed to its differentiation:

Then, we compute 

Finally, at h=2:

Best regards.
Answer:
The reactive nucleophile is Ketone.
Explanation:
In organic chemistry, The process of acid - catalyzed aldol condensation starts from when ketone (or any aldehyde) is converted to an -enol, after which it attacks another ketone/aldehyde that has already been activated by parbonyl oxygen protonation.
The process of this is that first of all the ketone undergoes tautomerization to form -enol. Thereafter, the other carbonyl will undergo protonation which makes the carbon activated towards attack. Now, the nucleophilic enol will be added to the carbonyl in a [1,2]-addition reaction and we will now use deprotonation to obtain the neutral Aldol product.
Now, since only the ketone can produce an -enol, thus it is the nucleophile as aldehydes are better electrophiles
Answer:
I believe that it is the 2nd option.
Explanation:
My reasonings are because C4H10O has 7 isomers. In which 4 are alcohol and the other 3 are ether.
The first option is ethers, specifically ethoxyethane.
The third option is ethers, specifically 1-methoxypropane.
The fourth option is an alcohol, specifically 1- butanol.
Therefore, leads us to the 2nd option that it is NOT an isomer of C4H10O
Answer:
one in a 2s orbital
Explanation:
Because of the peak near the nucleus in the 2s curve there is a higher probability of finding a 2s within 4 Å of the nucleus. In a multi-electron atom an electron in a 2s orbital will have a lower energy than one in a 2p orbital