Cleavage of Carbon-Carbon Bonds With Periodic Acid

Cleavage of Carbon-Carbon Bonds With Periodic Acid

Assessment

Interactive Video

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Biology, Chemistry, Science, Engineering

11th Grade - University

Hard

The video tutorial by Professor Dave explains the importance of forming and cleaving carbon-carbon bonds in organic synthesis. It introduces Periodic acid as a reagent that acts as an oxidizing agent, particularly useful for oxidizing polyhydroxy compounds like vicinal diols. The tutorial provides examples with glycerol and glyceraldehyde, demonstrating how Periodic acid cleaves carbon-carbon bonds to form carbonyls. The mechanism involves the formation of a cyclic periodate ester, leading to the cleavage of bonds and formation of iodic acid and water. This technique is valuable for breaking molecules into fragments or converting cyclic substrates to linear ones.

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7 questions

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1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why is forming and breaking carbon-carbon bonds crucial in organic synthesis?

To alter the color of organic molecules

To assemble and isolate specific molecular fragments

To change the state of matter of compounds

To increase the molecular weight of compounds

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What role does Periodic acid play in organic reactions?

It serves as a reducing agent

It acts as a Bronsted-Lowry acid

It functions as an oxidizing agent

It acts as a catalyst

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What happens when Periodic acid reacts with a vicinal diol?

It reduces the diol to an alkane

It forms a cyclic ether

It cleaves the carbon-carbon bond to form two carbonyls

It forms a single carbonyl compound

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How many equivalents of Periodic acid are needed to fully react with glycerol?

Four equivalents

Three equivalents

Two equivalents

One equivalent

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the product when dihydroxyacetone is oxidized by Periodic acid?

Ethanol

Acetone

Carbon dioxide

Methanol

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the key intermediate formed during the reaction of Periodic acid with vicinal diols?

Cyclic anhydride

Cyclic ether

Cyclic ketone

Cyclic periodate ester

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What drives the cleavage of carbon-carbon bonds in the mechanism of Periodic acid?

The formation of a cyclic anhydride

The strength of carbonyl bonds

The formation of a cyclic ether

The release of hydrogen gas