Optical Activity and Epimers Quiz
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Questions and Answers

What is the purpose of using OsO4 in the hydroxylation reaction of alkenes?

  • To prevent further oxidation of the glycol
  • To avoid using expensive reagents
  • To give a higher yield (correct)
  • To make the reaction less toxic

Why are gem diols unstable in aqueous solutions?

  • They react with water to form stable cyclic compounds
  • Due to the presence of water promoting dehydration to form aldehydes or ketones (correct)
  • Gem diols are inherently unstable compounds
  • Because aqueous solutions catalyze their conversion to alkenes

In the Pinacol-Pinacolone rearrangement, what is the main purpose of the protonation step?

  • To promote the 1,2-rearrangement
  • To initiate the formation of carbocation (correct)
  • To catalyze the dehydration of glycols
  • To stabilize the gem diols

Why is OsO4 used in catalytic amounts in the hydroxylation reaction of alkenes?

<p>Due to its high toxicity and volatility (C)</p> Signup and view all the answers

What is the outcome of treating epoxides with aqueous acid?

<p>Formation of a trans 1,2-diol (D)</p> Signup and view all the answers

Which compound is formed when gem diols dehydrate in the absence of water?

<p>Ketone (A)</p> Signup and view all the answers

What role does sodium bisulfate play in the OsO4-catalyzed formation of diols from alkenes?

<p>Catalyzes the formation of trans 1,2-diols (C)</p> Signup and view all the answers

What is the primary reason for using catalytic amounts of osmium tetraoxide (OsO4) in reactions?

<p>High toxicity and volatility (D)</p> Signup and view all the answers

'The alkene is treated with osmium tetraoxide, followed by sodium bisulfate' - What is the purpose of treating with sodium bisulfate in this sequence?

<p>To neutralize excess acid (D)</p> Signup and view all the answers

What is the consequence of using KMnO4 for oxidation of alkenes?

<p>Low yields due to further oxidation of functional groups (A)</p> Signup and view all the answers

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