An element or compound which occurs naturally in the earth is a mineral
Answer:
6
Explanation:
FCC is face centered cubic lattice. In FCC structure, there are eight atoms at the eight corner of the cubic unit cell and one atom centered in each of the faces. FCC unit cells consist of four atoms, (8/8) at the corners and (6/2) in the faces.
Given that, Cu has FCC structure and it contains a vacancy at origin (0, 0, 0). And there is no other vacancy directly adjacent to the vacancy at the origin. So, all the adjacent positions contain Cu atoms. Hence, the total number of adjacent atoms of the vacancy at origin can jump into this vacancy.
the above FCC unit cell clearly indicates that there are six adjacent atoms adjacent to the vacancy at origin
So, the total number of adjacent atoms of the vacancy at origin can jump into this vacancy is 6.
Answer: Option (b) is the correct answer.
Explanation:
Vitamins which are soluble in water are known as water-soluble vitamins. And, vitamins which remain insoluble in water are known as water-insoluble vitamins.
Water-soluble vitamins are able to be easily excreted by the human body through urine. For example, vitamin C and vitamin B-complex are water soluble vitamins.
Thus, we can conclude that water-soluble vitamins are easily excreted in the urine.
Answer:
i think d is the answer for this
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
