CSIR NET Chemical Science Exam > CSIR NET Chemical Science Videos > CSIR NET Crash Course for Chemical Science > Protecting Groups
Protecting Groups Video Lecture | CSIR NET Crash Course for Chemical Science - CSIR NET Chemical Science
FAQs on Protecting Groups Video Lecture - CSIR NET Crash Course for Chemical Science - CSIR NET Chemical Science
| 1. What are protecting groups in organic chemistry? |  |
Ans. Protecting groups are functional groups that are temporarily added to certain reactive sites on a molecule to prevent unwanted reactions from occurring at those sites during a chemical reaction.
| 2. Why are protecting groups used in organic synthesis? | |
Ans. Protecting groups are used in organic synthesis to selectively control the reactivity of specific functional groups within a molecule, allowing for the synthesis of complex molecules without unwanted side reactions.
| 3. How are protecting groups removed after the desired reaction is complete? | |
Ans. Protecting groups can be removed by using specific reagents or conditions that selectively cleave the protecting group from the molecule without affecting the rest of the structure.
| 4. What are some common protecting groups used in organic chemistry? | |
Ans. Some common protecting groups include tert-butyldimethylsilyl (TBDMS), benzyl (Bn), tert-butoxycarbonyl (Boc), and acetyl (Ac), among others.
| 5. What are the challenges associated with using protecting groups in organic synthesis? | |
Ans. Some challenges of using protecting groups include the need for additional synthetic steps, the potential for side reactions during deprotection, and the possibility of introducing impurities into the final product.
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Dec 23, 2024 Last updated |
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