Correct answer: B. Paleozoic. I took the test and it was right.
Answer:
I do not know the Answer I'm just trying to get my point
Explanation:
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Answer:
2,2,3,3-tetrapropyloxirane
Explanation:
In this case, we have to know first the alkene that will react with the peroxyacid. So:
<u>What do we know about the unknown alkene? </u>
We know the product of the ozonolysis reaction (see figure 1). This reaction is an <u>oxidative rupture reaction</u>. Therefore, the double bond will be broken and we have to replace the carbons on each side of the double bond by oxygens. If
is the only product we will have a symmetric molecule in this case 4,5-dipropyloct-4-ene.
<u>What is the product with the peroxyacid?</u>
This compound in the presence of alkenes will produce <u>peroxides.</u> Therefore we have to put a peroxide group in the carbons where the double bond was placed. So, we will have as product <u>2,2,3,3-tetrapropyloxirane.</u> (see figure 2)
Answer:
Compound A is succinic anhydride and B is methyl succinate (the monomethyl ester).
Structural Diagram is attached.
Explanation:
A.
Succinic anhydride appears as colorless needles or white crystalline solid. ... Succinic anhydride, also called dihydro-2, 5-furandione, is an organic compound with the molecular formula C4H4O3. It is the acid anhydride of succinic acid.
B.
Monomethyl succinate is a dicarboxylic acid monoester that is succinic acid in which one of the carboxy groups has been converted to its methyl ester. It is a dicarboxylic acid monoester and a hemisuccinate. ... They have the general structure RC(=O)OR', where R=fatty aliphatic tail or organyl group and R'=methyl group.