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Search options not deleted user 92858

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.

1 vote
0 answers
68 views

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 …
Loveforphysics's user avatar
-1 votes
1 answer
91 views

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 …
Loveforphysics's user avatar
0 votes
0 answers
412 views

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 …
Loveforphysics's user avatar
1 vote
0 answers
49 views

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 …
Loveforphysics's user avatar