Modify the structure to draw the organic product of the following reaction. Note that [O] is present in excess. Draw the sulfur‑containing product of the oxidation reaction between two 2‑methyl‑1‑propanethiol molecules. Include all hydrogen atoms.
Lipids
The heterogeneous classes of organic compounds that are not water-soluble but are dissolved in organic solvents that are non-polar in nature are termed lipids. They are a long chain of fatty acids and esters of alcohols. Lipids are generally seen in several plants, microorganisms, and animals. They are utilized as insulation, components of the cell membrane, hormones, and molecules for the storage of energy.
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.
Structure Of Camphor
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.
Glycolipid In Organic Chemistry
Glycolipids are lipids that are an important class of organic compounds in chemistry that have simple to complex applications. They contain carbohydrates, fatty acids, sphingolipids or a glycerol group. In other words, they are the modifications of lipids like acylglycerols, prenols and ceramides. They are all part of a wider group of compounds known as glycoconjugates.
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.
Modify the structure to draw the organic product of the following reaction. Note that [O] is present in excess.
Draw the sulfur‑containing product of the oxidation reaction between two 2‑methyl‑1‑propanethiol molecules. Include all hydrogen atoms.
![**Title: Modifying Chemical Structures to Represent Products**
In this educational task, you are asked to modify a given molecular structure to represent the product of a chemical reaction.
**Reaction:**
\[ \text{CH}_3\text{CHOHCH}_3 \xrightarrow{[O]} \]
**Instruction Panel:**
- **Select**: Choose the molecular structure elements.
- **Draw**: Options for adding bonds and atoms.
- **Bonds**: Single, double, and triple bonds.
- **Atoms**: Add carbon (C), hydrogen (H), and oxygen (O).
- **Rings**: Options for drawing cyclic structures.
- **More**: Additional drawing options.
- **Erase**: Function to remove elements from the structure.
**Current Structure:**
A simple molecular diagram of 2-propanol (the reactant), featuring:
- A central carbon (C) atom connected vertically to an oxygen (O) with a single bond, forming an alcohol group.
- Two more carbon atoms (C) connected horizontally with single bonds.
- Hydrogen atoms (H) attached to each carbon to complete their valency.
**Task Objective:**
Modify this structure to reflect the expected product of the oxidation of 2-propanol, which typically results in the formation of acetone (propanone). This involves the transformation of the -OH group into a carbonyl group (C=O).
Use the drawing tools provided to complete the task and accurately depict the structural transformation.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F4ff03bd5-cd77-4623-a6f4-279a50800fd2%2Fb4f38770-fc32-4fe4-bd8c-049163bf0a90%2Fif2zol6_processed.png&w=3840&q=75)
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