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PCC, or pyridinium chlorochromate, acts as an oxidizing agent in chemical reactions. It helps to facilitate the transfer of electrons between reactants, leading to the conversion of one substance into another.

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6mo ago

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When Pyridium chlorochromate is added to primary alcohol what does it give?

when u add PCC to a primary alcohol its gets oxidized to an aldehyde. example CH3CH2CH2OH +PCC --. CH3CH2COOH when u add PCC to a primary alcohol its gets oxidized to an aldehyde. example CH3CH2CH2OH +PCC --. CH3CH2COOH


What are the key arguments presented in the case of Jones vs PCC?

In the case of Jones vs PCC, the key arguments revolve around the issue of privacy rights and the extent to which an individual's personal information can be disclosed without their consent. The plaintiff, Jones, argues that the PCC violated her privacy by sharing her personal information without permission, while the PCC contends that they were justified in doing so for legal or public interest reasons. The case raises important questions about the balance between privacy rights and the need for information disclosure in certain circumstances.


What is the product of the reaction of 2-methylcyclohexanol under acidic conditions?

1. Add Al2O3 at 400 deg C to eliminate the -OH and form 1-methylcyclohexene 2. Add BH3 in THF, then H2O2 in OH- to add an -OH group to the less substituted carbon of the alkene mentioned above (hydroboration-oxidation is anti-Markovnikoff) 3. Add PCC in CH2Cl2 to form your ketone. I think. Came across this question myself and this is how i solved it. Not 100% sure if its correct though


What are the Reactions of ethanal with potassium permanganate?

Ethanol (CH3CH2OHl) + KMnO4 ----> Ethanal (CH3CHO) -----> Ethanoic Acid (CH3COOH) Primary Alcohol Oxidized ---> Aldehyde Oxidized---> Carboxyilic Acid You could attain Ethanal by using the oxidizing agent Pyridinium Chlorochromate (PCC) anhydrously.


What is the equation for the oxidation of a primary alcohol?

primary alcohols become produce aldehydes when oxidized and carboxylic acid upon further oxidation. secondary alcohol oxidation produces ketone. while tertiary alcohols has no reaction except if combustion is applied.