When it is treated with sodium ethoxide in deuterated ethanol (C2H5OD), cyclopentadiene exchanges all of its hydrogens for deuterium. Draw a structure for the intermediate in this reaction with all protons (no deuterons).
When it is treated with sodium ethoxide in deuterated ethanol (C2H5OD), cyclopentadiene exchanges all of its hydrogens for deuterium. Draw a structure for the intermediate in this reaction with all protons (no deuterons).
Chemistry
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Chapter1: Chemical Foundations
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When it is treated with sodium ethoxide in deuterated ethanol (C2H5OD), cyclopentadiene exchanges all of its hydrogens for deuterium.
Draw a structure for the intermediate in this reaction with all protons (no deuterons).

Transcribed Image Text:### Transcription and Explanation
#### Chemical Reaction
The image illustrates a chemical reaction involving the conversion of cyclopentadiene to a deuterated cyclopentadiene.
- **Reactant:** Cyclopentadiene (C₅H₆)
- Structure: A five-membered carbon ring with two conjugated double bonds (a diene) and one hydrogen atom attached to each carbon in the ring.
- **Reagent:** Sodium ethoxide in deuterated ethanol (NaOC₂H₅/C₂H₅OD)
- This reagent is used to exchange hydrogen atoms with deuterium atoms.
- **Product:** Deuterated Cyclopentadiene (C₅D₆)
- Structure: Similar five-membered carbon ring with two conjugated double bonds. Each hydrogen atom in the original compound is substituted with a deuterium atom, represented by "D".
#### Reaction Mechanism
The reaction involves the deprotonation of cyclopentadiene to form a cyclopentadienyl anion, followed by the exchange of hydrogen atoms for deuterium atoms due to the presence of NaOC₂H₅/C₂H₅OD.
This reaction is an example of a deuterium exchange process, often used in organic chemistry to incorporate deuterium into molecules for studying reaction mechanisms or for use in spectroscopy.
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