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Use this tag for questions relating to organic molecules and their properties (structure of organic molecules, spectroscopic properties, reaction mechanisms, stereochemistry etc). DO NOT use this tag as the only tag in your question, as this tag by itself cannot appropriately classify your question. Always use this tag in addition to other more specific tags.
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Poisoned catalysts
CaCO3 in rosenmund reduction, lead in Lindlar's catalyst, or steel in Raney nickel all act as poisins but the carbon in Pd/C is just for support. How do the others affect the catalytic activity but no …
-1
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1
answer
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Are glycosides stable to acidic hydrolysis? [closed]
I recently read a fact about glycosides:
Strong reagents like $\ce{C6H5NHNH2}$ or $\ce{NH2OH}$ are required to decompose it and acidic hydrolysis fails to do so.
Why is it so? What makes it differen …
0
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0
answers
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Chiral carbons in glucose
In the open chain structure of glucose, one can identify 4 chiral carbon atoms but some sources consider the ring structure and then say that glucose has 5 chiral carbon atoms. If asked to state the n …
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0
answers
49
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Reduction of (4-methylcyclohex-3-en-1-yl)methoxymethylbenzene to 4-methylcyclohex-3-en-1-ol
Find the suitable reagent to carry out the following transformation:
The answer provided says that $\ce{H2/Pd-C}$ can be used to bring about the given transformation, but I am failing to understand …