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Glucose on treatment with sodium amalgam...

Glucose on treatment with sodium amalgam gives

A

n-heptanoic acid

B

Sorbitol

C

gluconic acid

D

glucaric acid

Text Solution

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The correct Answer is:
To solve the question "Glucose on treatment with sodium amalgam gives," we will follow these steps: ### Step 1: Understand the Structure of Glucose Glucose is a simple sugar (monosaccharide) with the molecular formula C6H12O6. It contains an aldehyde group (-CHO) and several hydroxyl groups (-OH). The structure can be represented as follows: - Aldehyde group: -CHO - Hydroxyl groups: -OH (attached to various carbon atoms) ### Step 2: Identify the Reactant When glucose is treated with sodium amalgam (Na/Hg), sodium acts as a reducing agent. Sodium amalgam is a mixture of sodium and mercury, and it is commonly used in organic chemistry for reduction reactions. ### Step 3: Determine the Reaction In this reaction, the aldehyde group (-CHO) of glucose is reduced to a primary alcohol (-CH2OH). This reduction process converts glucose into sorbitol. ### Step 4: Write the Product After the reduction of glucose, the product formed is sorbitol, which has the following structure: - Sorbitol structure: - All carbon atoms will have -CH2OH groups instead of the aldehyde group. - The structure will look like this: ``` CH2OH | HO-CH | HO-CH | HO-CH | HO-CH | CH2OH ``` ### Conclusion Thus, when glucose is treated with sodium amalgam, the product formed is **sorbitol**. ### Final Answer: Glucose on treatment with sodium amalgam gives **sorbitol**. ---

To solve the question "Glucose on treatment with sodium amalgam gives," we will follow these steps: ### Step 1: Understand the Structure of Glucose Glucose is a simple sugar (monosaccharide) with the molecular formula C6H12O6. It contains an aldehyde group (-CHO) and several hydroxyl groups (-OH). The structure can be represented as follows: - Aldehyde group: -CHO - Hydroxyl groups: -OH (attached to various carbon atoms) ...
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Knowledge Check

  • Acetone on treatment with sodium and ethanol gives

    A
    aceticacid
    B
    propanol
    C
    1-propanol
    D
    isopropyl alcohol
  • Ethyl iodide on treatment with sodium methoxide gives

    A
    `CH_3-O-CH_3`
    B
    `C_2H_5OCH_3`
    C
    `C_2H_5OC_2H_5`
    D
    `C_2H_6`
  • D-Glucose upon treatment with bromine-water gives :

    A
    B
    C
    D
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