Answer:
The procedure you will use in this exercise exploits the difference in acidity and solubility just described.
(a) you will dissolve your unknown in ethyl acetate (an organic solvent). All of the possible compounds are soluble in ethyl acetate.
(b) you will extract with sodium bicarbonate to remove any carboxylic acid that is present.
(c) you will extract with sodium hydroxide to remove any phenol that is present.
(d) you will acidify both of the resulting aqueous solutions to cause any compounds that were extracted to precipitate.
The 18o-labeled methanol (CH3O*H) will appear in the products side at position b.
<h3>
Position of 18o-labeled methanol in the products</h3>
The 18O label will appear at position b in the product as indicated in the image.
This methoxy group in the product formed in position b comes from the 18O-labeled methanol (CH3OH).
While the oxygens at positions a and c in the product come from the unlabeled hemiacetal.
Thus, the 18o-labeled methanol (CH3O*H) will appear in the products side at position b.
Learn more about methanol here: brainly.com/question/17048792
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Answer:
The answer to your question is below
Explanation:
11. Alkali metals
12. Halogens
13. Transition metals
14. Halogens
15. Noble gases
16. Alkaline earth metals
17. Transition metals
18. Alkaline earth metals
19. Transition metals
20. Alkali metals
21.- Periods
22.- Calcium
23.- Iodine, I
24.- A. atomic number
Answer:
Change in internal energy (ΔU) = -9 KJ
Explanation:
Given:
q = –8 kJ [Heat removed]
w = –1 kJ [Work done]
Find:
Change in internal energy (ΔU)
Computation:
Change in internal energy (ΔU) = q + w
Change in internal energy (ΔU) = -8 KJ + (-1 KJ)
Change in internal energy (ΔU) = -8 KJ - 1 KJ
Change in internal energy (ΔU) = -9 KJ
