Answer:
<u>Optical purity = 76.9231 %</u>
<u>Specific rotation of mixture = - 97.6923 °</u>
Explanation:
The mass of the racemic mixture = 3 g
It means it contains R enantiomer = 1.5 g
S enantiomer = 1.5 g
Amount of Pure R = 10 g
Total R = 11.5 g
Total volume = 500 mL + 500 mL = 1000 mL = 1 L
[R] = 11.5 g/L
[S] = 1.5 g/L
Enantiomeric excess =
=
= 76.9231 %
<u>Optical purity = 76.9231 %</u>
Also,
Optical purity = 
Optical rotation of pure enantiomer = −127 °

<u>Specific rotation of mixture = - 97.6923 °</u>
Answer:
0.025M
Explanation:
As you must see in your graph, each concentration of the experiment has an absorbance. Following the Beer-Lambert's law that states "The absorbance of a solution is directely proportional to its concentration".
At 0.35 of absorbance, the plot has a concentration of:
<h3>0.025M</h3>
Answer:
16 cm
Explanation:
Because when you look at the ruler, it shows the length as 16 cm
Answer:
those things that looks like cristals
Answer
2-methyl-2-pentene
Explanation:
1. Identify the group that takes precedence in this case alkene hence this molecule is an alkene with a methyl group side chain.
2.Find the longest carbon chain where the functional group(alkene group in this case) has the lowest Carbon number
3.What are the side groups? One side group can be seen at carbon 2 this group is methyl
4. Naming, number separated by "," and number from letters by "-" so the compound should be
2-methyl-2-pentene