help 3. Show the mechanism (curved arrows) for the two transformations shown below. Use H30* as...

Question

Question

help

Answer 1

Answer #1

Solution=

First mechanism is the deprotection of the aldehyde to form ethanal and diol. All the step are reversible in nature.

Second mechanism is the intramolecular ester formation reaction and all steps are reversible.

Answer 2

Similar Homework Help Questions

show the mechanism with curved arrows for the two transformations shown below using H30 plus as...

show the mechanism with curved arrows for the two transformations shown below using H30 plus as a catalyst 3. Show the mechanism (curved arrows) for the two transformations shown below. Use H30 as a catalyst. mechanism 1 mechanism 2 OH НО OH HO OH Page 2 of 4
3. Show the mechanism (curved arrows) for the two transformations shown below. Use H30' as a...

3. Show the mechanism (curved arrows) for the two transformations shown below. Use H30' as a catalyst. mechanism mechanism 2 e =0 OH HO OH OH HO
Show the mechanism (curved arrows) for the two transformations shown below. Use H30+ as a catalyst....

Show the mechanism (curved arrows) for the two transformations shown below. Use H30+ as a catalyst. mechanism 1 mechanism 2 ОН HO OH OH НО

3. Mechanisms: Provide a detailed, stepwise mechanism for the following transformations. Use curved arrows to show...

3. Mechanisms: Provide a detailed, stepwise mechanism for the following transformations. Use curved arrows to show the movement of electrons. do 10.♡.
3. Mechanisms: Provide a detailed, stepwise mechanism for the following transformations. Use curved arrows to show...

3. Mechanisms: Provide a detailed, stepwise mechanism for the following transformations. Use curved arrows to show the movement of electrons. Me Me Me TSOH -Me Me 120 °C OH
1) Draw a rational mechanism for the reaction shown below. Use curved arrows appropriately. Show all...

1) Draw a rational mechanism for the reaction shown below. Use curved arrows appropriately. Show all relevant intermediate(s) and lone pairs of electrons and formal charges where appropriate. HO H2SO4 Ome

Use curved arrows to show the mechanism of the step below

Use curved arrows to show the mechanism of the step below. Make the ends of your arrows specify the origin and destination of reorganizing electrons. Use curved arrows to show the mechanism of the step below. If more than one resonance form of the product is possible, show the most stable form.
Use curved arrows to show the mechanism of the step below. Make the ends of your...

Use curved arrows to show the mechanism of the step below. Make the ends of your arrows specify the origin and destination of reorganizing electrons. Base : H--0: :OH HO +1ニ11110.
Use curved arrows to show the mechanism of the step below.

Use curved arrows to show the mechanism of the step below. Make the ends of your arrows specify the origin and destination of reorganizing electrons.

3. Write a complete, stepwise mechanism to account for each of the following transformations. Use...

3. Write a complete, stepwise mechanism to account for each of the following transformations. Use curved arrows to denote electron flow. a. (7 points) 18 H2018 Ht catalyst a. (3 points) NaN3 CI N3 NaCI 3. Write a complete, stepwise mechanism to account for each of the following transformations. Use curved arrows to denote electron flow. a. (7 points) 18 H2018 Ht catalyst a. (3 points) NaN3 CI N3 NaCI