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:
n=N/Na
n = \frac{8.23 \times {10}^{22} }{6.02 \times {10}^{23} } = 0.1367 \: mol
answer: 0.14 mol
Explanation:
I’m distilled water all of the dissolved substances mixed in water have been removed by evaporation.
Active sites in enzymes are where substrates bind. Once they bind, a catalytic reaction occurs as a complex between substrate and enzyme is formed. Enzymes are termed as biocatalysts or simply catalysts since they speed up the catalytic reaction. After the reaction, they simply revert back to their original form, after having adjusted to fit with substrate.