HW 10 #4 **Be sure to answer all parts.****Part 1:**Predict the product of the following reaction.**Reaction Scheme:**- Starting material: A linear hydrocarbon chain with a terminal double bond.- Reagent: BH₃ (1 equivalent) in ether.- Product: A hydrocarbon chain with a hydroxyl group (BH₂) added to the less substituted carbon of the double bond, indicating hydroboration-oxidation.**Diagram:**- The left side shows the reactant, a 1-hexene molecule.- The right side displays the reaction product, showing the addition of BH₂.*View structure button below the product.***Part 2 out of 2:**Draw a stepwise mechanism.**Diagram:**- Initial structure: 1-hexene and BH₃ molecules.- Transition arrow pointing to an empty structure box for illustrating the mechanism.*Edit structure buttons are available for modifying steps in the reaction mechanism.*

Alkene gives an electrophilic addition reaction with borane. Alkene reacts with BH3 and then NaOH and H2O2 to form an alcohol. This reaction is an anti-Markovnikov reaction, with the hydroxyl group attaching to the less-substituted carbon of double bond.The hydroboration–oxidation reaction is a stereospecific two-step hydration reaction. This reaction results in the syn addition of hydrogen and a hydroxyl group at the double bond of an alkene.The vacent orbital of boron reacts with the pi-electrons of alkene and the hydrogen atom with its electron pairs add to the carbon atom. The reaction is process in a single step.The stepwise mechanism is as follows:

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Be sure to answer all parts. Part 1: Predict the product of the following reaction. Part 2 out of 2 Draw a stepwise mechanism. edit structure www BH3 (1 equiv) ether BH₂ view structure edit structure ...

Be sure to answer all parts. Part 1: Predict the product of the following reaction. Part 2 out of 2 Draw a stepwise mechanism. edit structure www BH3 (1 equiv) ether BH₂ view structure edit structure ...

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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HW 10 #4

**Be sure to answer all parts.**

**Part 1:**

Predict the product of the following reaction.

**Reaction Scheme:**
- Starting material: A linear hydrocarbon chain with a terminal double bond.
- Reagent: BH₃ (1 equivalent) in ether.
- Product: A hydrocarbon chain with a hydroxyl group (BH₂) added to the less substituted carbon of the double bond, indicating hydroboration-oxidation.

**Diagram:**
- The left side shows the reactant, a 1-hexene molecule.
- The right side displays the reaction product, showing the addition of BH₂.

*View structure button below the product.*

**Part 2 out of 2:**

Draw a stepwise mechanism.

**Diagram:**
- Initial structure: 1-hexene and BH₃ molecules.
- Transition arrow pointing to an empty structure box for illustrating the mechanism.

*Edit structure buttons are available for modifying steps in the reaction mechanism.*

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