Problem 46
Question
On reacting with oxalic acid at \(503 \mathrm{~K}\), glycerol gives (a) formic acid (b) glyceraldehyde (c) allyl alcohol (d) none of these
Step-by-Step Solution
Verified Answer
The correct product is (c) allyl alcohol.
1Step 1: Understanding the reaction
Glycerol, a trihydric alcohol (also known as glycerine), when reacted with oxalic acid at high temperature (around \(503 \text{ K}\)), undergoes a dehydration reaction. The key is to examine if this reaction is known and to identify the products that typically result.
2Step 2: Identify possible products
During the heating of glycerol with oxalic acid, a dehydration process can yield several possible products: one of which is allyl alcohol. It is important to note that the conditions specified, namely the high temperature of \(503 \text{ K}\), favor this typical dehydration product.
3Step 3: Evaluating the options
Review the options provided: (a) formic acid, (b) glyceraldehyde, (c) allyl alcohol, (d) none of these. Considering the identified reaction, the product formed by this specific dehydration process is allyl alcohol. This matches option (c).
4Step 4: Conclusion
Determining the accurate option means confirming allyl alcohol as the correct answer when glycerol is reacted with oxalic acid at \(503 \text{ K}\). Thus, the choice is found among the given options.
Key Concepts
Dehydration ReactionAllyl Alcohol FormationOrganic Chemistry
Dehydration Reaction
In chemistry, a dehydration reaction is a type of chemical reaction that typically involves the removal of water from a molecule. It's like squeezing out moisture to form a new, different substance. This process is especially common with alcohols, like glycerol, where the hydroxyl groups (\( -OH \)) can lose a water molecule. By applying heat or a catalyst, a dehydration reaction can lead to the creation of unsaturated compounds. In the example of glycerol reacting with oxalic acid at \( 503 \text{ K} \), this high temperature provides the necessary energy for the dehydration reaction to occur.
- This reaction results in the loss of water molecules.
- Leads to the formation of new products, which are often unsaturated compounds.
- Usually requires heat or another form of energy to proceed.
Allyl Alcohol Formation
During the dehydration reaction of glycerol with oxalic acid, one major product formed is allyl alcohol. Allyl alcohol is an organic compound characterized by its functional group \( CH_2=CH-CH_2OH \), making it an unsaturated alcohol. The formation of allyl alcohol illustrates how dehydration can alter a compound's structure by creating a double bond.
- Occurs typically when glycerol loses water to form a double bond.
- The resulting allyl alcohol has a distinct smell – sometimes recognized in nature as it can be found in garlic.
- This compound serves as a valuable intermediate in various chemical synthesis processes, including the production of pharmaceuticals and fragrances.
Organic Chemistry
Organic chemistry is the study of carbon-containing compounds and their reactions. It's foundational to understanding biological molecules and the myriad of reactions they can undergo. In the realm of organic chemistry, reactions like the one between glycerol and oxalic acid provide a microcosm of study into how molecules interact. Organic chemistry facilitates the synthesis of new materials, enhances understanding of biological processes, and more.
- Covers the reactions, composition, structure, and synthesis of carbon-based compounds.
- Helps in understanding the properties of substances ranging from simple gases to complex polymers.
- Leverages reactions such as dehydration to explore the transformations these molecules can undergo.
Other exercises in this chapter
Problem 43
Which of the following reactions does not yield an alkyl halide? (a) diethyl ether \(+\mathrm{RCOCl}\) (b) diethyl ether \(+\mathrm{PCl}_{5}\) (c) diethyl ether
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When benzenediazonium chloride is treated with water, the compound formed is (a) \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COOH}\) (b) \(\mathrm{C}_{6} \mathrm{H}
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Ether is obtained by the reaction of ethyl alcohol and \(\mathrm{H}_{2} \mathrm{SO}_{4}\) at (a) \(474 \mathrm{~K}\) (b) \(383 \mathrm{~K}\) (c) \(413 \mathrm{~
View solution Problem 48
Ether is obtained by the reaction of ethyl alcohol and \(\mathrm{H}_{2} \mathrm{SO}_{4}\) at (a) \(474 \mathrm{~K}\) (b) \(383 \mathrm{~K}\) (c) \(413 \mathrm{~
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