How do you explain the absence of aldehyde group in the pentaacetate of D-glucose?
D-glucose reacts with hydroxylamine (NH2OH) to form an oxime because of the presence of aldehydic (-CHO) group or carbonyl carbon. This happens as the cyclic structure of glucose forms an open chain structure in an aqueous medium, which then reacts with NH2OH to give an oxime.
But pentaacetate of D-glucose does not react with NH2OH. This is because pentaacetate does not form an open chain structure.
The reaction between A and B is first order with respect to A and zero order with respect to B. Fill in the blanks in the following table:
| Experiment |
A/ mol L - 1 |
B/ mol L - 1 |
Initial rate/mol L - 1 min - 1 |
| I | 0.1 | 0.1 |
2.0 × 10 - 2 |
| II | -- | 0.2 |
4.0 × 10 - 2 |
| III | 0.4 | 0.4 | -- |
| IV | -- | 0.2 |
2.0 × 10 - 2 |
NCERT questions are designed to test your understanding of the concepts and theories discussed in the chapter. Here are some tips to help you answer NCERT questions effectively:
D-glucose reacts with hydroxylamine (NH2OH) to form an oxime because of the presence of aldehydic (-CHO) group or carbonyl carbon. This happens as the cyclic structure of glucose forms an open chain structure in an aqueo...
Step-by-step explanation:
• D-glucose reacts with hydroxylamine (NH2OH) to form an oxime because of the presence of aldehydic (-CHO) group or carbonyl carbon
• This happens as the cyclic structure of glucose forms an open chain structure in an aqueous medium, which then reacts with NH2OH to give an oxime
•
•
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This question is important because it tests key concepts from the NCERT syllabus and is frequently asked in CBSE exams.
This question is based on core NCERT concepts explained in the chapter and should be revised thoroughly before exams.
Students often lose marks by skipping steps, writing incomplete explanations, or misunderstanding keywords used in the question.
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