Organic Chemistry Synthesis Challenge 1

The video tutorial discusses the transformation of cyclopentene into a target molecule with additional functionality. It covers the introduction of functional groups, focusing on achieving trans stereochemistry through epoxidation and SN2 reactions. The tutorial also explains the use of Williamson Ether Synthesis to complete the transformation, highlighting the importance of stereochemistry and functional group introduction.

What is the starting material mentioned in the problem?

• Cyclohexane

• Cyclopentene

• Benzene

• Ethylene

Which functional group is identified as a great nucleophile?

• CN group

• COOH group

• OH group

• NH2 group

What is the significance of trans stereochemistry in this reaction?

• It allows for the introduction of a hydroxyl group.

• It ensures the correct spatial arrangement of atoms.

• It prevents the formation of a three-membered ring.

• It ensures the molecule is planar.

Which reagent is suggested for epoxidation?

• Grignard reagent

• Lithium aluminum hydride

• MCPBA

• Sodium hydride

What type of reaction is used to introduce the nitrile group?

• E2 reaction

• SN2 reaction

• E1 reaction

• SN1 reaction

Which synthesis method is used to convert a hydroxyl group to an ether?

• Claisen condensation

• Williamson Ether Synthesis

• Aldol condensation

• Friedel-Crafts acylation

What is the role of sodium hydride in the final steps?

• It deprotonates the hydroxyl group.

• It acts as a nucleophile.

• It reduces the nitrile group.

• It forms a carbocation.