Write chemical reactions involved in Cannizzaro Reaction of Methanal
The Cannizzaro reaction is a classic redox process where non-enolizable aldehydes, which lack an \(\alpha\)-hydrogen, are treated with a strong base (\(\text{NaOH}\)) to undergo disproportionation. This reaction results in the simultaneous formation of an alcohol and a carboxylate salt.
Consider the reaction with methanal (formaldehyde): \[ 2\text{HCHO} + \text{NaOH} \rightarrow \text{HCOO}^- \text{Na}^+ + \text{CH}_3\text{OH} \]
The spin-only magnetic moment of \( \text{Cr}^{3+} \) cation is ___________.
The linkage present in Lactose is ___________.
The pH of a 0.001 M HCl solution is ___________
Write chemical reactions involved in Rosenmund Reduction
Write chemical reactions involved in Gattermann-Koch Formylation