Draw a stepwise mechanism for the following reaction: Part 1 out of 4 H-Br finish structure ... OH HBr edit structure ... O HBr Br H₂O HO™ HOBr Br
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Glycerophospholipid
Glycerophospholipid is the most abundantly occuring phospholipids found in the biological membranes. Lipids include a group of organic compounds like fats, hormones, oils, waxes, vitamins etc. They are non-polar molecules and are insoluble in water. Lipids play an important role in biological systems. They are the building blocks of our cell membranes, store energy and are involved in signaling.
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A terpene with the molecular formula of C10H16O is a waxy, white color solid known as camphor. It is flammable. It also possesses a very pungent taste and a strong odor. There are various sources for extracting camphor from natural products such as the wood of the tree of camphor laurel. Sublimation of wood and steam distillation are some of the methods involved in obtaining camphor.
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Diterpenoid
The terpenoid class includes diterpenoids, which are chemical compounds with 20 carbon atoms. They are made up of four isoprene units and are derived from geranylgeraniol, a C20 precursor. They have a C20H32 basic structure. These characteristics distinguish diterpenoids from simple terpenes, which have just 10 carbon atoms.
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![### Educational Website Content
#### Reaction Mechanism for Alcohol and HBr
##### Objective:
Draw a stepwise mechanism for the reaction where an alcohol reacts with HBr to form an alkyl bromide.
**Reaction Equation:**
\[ \text{Alcohol} \, (\text{OH}) + \text{HBr} \rightarrow \text{Alkyl Bromide} \]
**Illustration:**
- **Reactants:** The starting compound is an alcohol with the -OH group attached to a carbon chain. It reacts with HBr.
- **Products:** The primary reaction product is an alkyl bromide where the bromine atom has replaced the hydroxyl group.
**Part 1 out of 4:**
- **Mechanistic Step:**
- The first part in the mechanism requires identifying the intermediate and the leaving group.
- The alcohol reacts with HBr, leading to the formation of a carbocation intermediate. The reaction is depicted with structural formulas.
- **Diagram Explanation:**
- **Left Structure:** Displays the starting compounds: an alcohol and HBr.
- **Middle Structure:** Shows the formation of a carbocation where the -OH group has left, indicating an incomplete structure needing further editing.
- **Right Section (Choices):** Options for the leaving group and other products are listed:
- \( \text{HBr} \)
- \( \text{Br}^- \) (Highlighted as correct)
- \( \text{H}_2\text{O} \)
- \( \text{HO}^- \)
- \( \text{HOB}_r \)
**Selection:**
The correct answer is marked, indicating the liberation of \( \text{Br}^- \) as the leaving group in this reaction step.
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This explanation demonstrates how the hydroxyl group in an alcohol is replaced by a bromine atom from HBr, resulting in alkyl bromide formation. Further steps will involve the completion of the mechanism, detailing carbocation stability and rearrangements if necessary.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fb0d45dce-c646-4e67-b264-22576bb4d853%2F81fd4181-781d-4129-a514-4553d2ddc90a%2F7ntwgrk_processed.png&w=3840&q=75)

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