Answer:
37 mmol of acetate need to add to this solution.
Explanation:
Acetic acid is an weak acid. According to Henderson-Hasselbalch equation for a buffer consist of weak acid (acetic acid) and its conjugate base (acetate)-
![pH=pK_{a}(acetic acid)+log[\frac{mmol of CH_{3}COO^{-}}{mmol of CH_{3}COOH }]](https://tex.z-dn.net/?f=pH%3DpK_%7Ba%7D%28acetic%20acid%29%2Blog%5B%5Cfrac%7Bmmol%20of%20CH_%7B3%7DCOO%5E%7B-%7D%7D%7Bmmol%20of%20CH_%7B3%7DCOOH%20%7D%5D)
Here pH is 5.31, 
(acetic acid) is 4.74 and number of mmol of acetic acid is 10 mmol.
Plug in all the values in the above equation:
![5.31=4.74+log[\frac{mmol of CH_{3}COO^{-}}{10}]](https://tex.z-dn.net/?f=5.31%3D4.74%2Blog%5B%5Cfrac%7Bmmol%20of%20CH_%7B3%7DCOO%5E%7B-%7D%7D%7B10%7D%5D)
or, mmol of 
= 37
So 37 mmol of acetate need to add to this solution.
I think it’s C but I’m not sure
ANSWER
The correct answer is A
EXPLANATION
Plants manufacture their on food by the process of photosynthesis. During this process, plants trap radiant energy from the sun by the help of chlorophyll in the leaves.
Radiant energy with other raw materials such as water, carbon dioxide and mineral salts is converted to food (in the form of starch) which contains chemical energy.
Answer:
Repeated SN2 reactions occur leading to the formation of a racemic mixture
Explanation:
S-2-iodooctane is a chiral alkyl halide with an asymmetric carbon atom. The presence of an asymmetric carbon atom implies that it can rotate plane polarized light and thus lead to optical isomerism. The two configurations of the compound are R/S according to the Cahn-Prelong-Ingold system.
However, when S-2-iodooctane is treated with sodium iodide in acetone, repeated SN2 reactions occur since the iodide ion is both a good nucleophile and a good leaving group. Hence a racemic modification is formed in the system with time hence we end up with (±)- Iodooctane.
