Answer:
(3R,4R)-4-bromohexan-3-ol
Explanation:
In this case, we have reaction called <u>halohydrin formation</u>. This is a <u>markovnikov reaction</u> with <u>anti configuration</u>. Therefore the halogen in this case "Br" and the "OH" must have <u>different configurations</u>. Additionally, in this molecule both carbons have the <u>same substitution</u>, so the "OH" can go in any carbon.
Finally, in the product we will have <u>chiral carbons</u>, so we have to find the absolute configuration for each carbon. On carbon 3 we will have an "R" configuration on carbon 4 we will have also an "R" configuration. (See figure 1)
I hope it helps!
Answer:
It is composed of 57.17% S and 42.83% C and has a molar mass of 448.70 g/mol. Determine the empirical and molecular formulas of “sulflower.”
...
what is the molecular formula of the compound?
Empirical formula Molar mass (g/mol) Molecular formula
CHO 116.1
C8H16
Explanation:
Hope this helps
Answer:
24m/s
Explanation:
a=change of v/change of t
6m/s^2=v/4s
multiply both sides by 4s
v=24m/s
Answer:
0.29
Explanation:
Since the name of the acid (and the equation) is not given, you must assume that it is a 1:1 ratio. Use equation: volume of acid x molarity of acid = volume of base x molarity of base (when the ratio is 1:1).