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Their website states that alconox has a pH 9.5 (alconox.com). So to answer your question, it is basic.
Wiki User
∙ 15y ago
Wiki User
∙ 14y ago"base" as it liberates OH ion
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Is formic acid an Aldehyde or a Carboxylic acid?
Formic acid is methanoic acid. A carboxylic acid.
An aldehyde forms a carboxylic acid by?
oxidation
Why glucose is used for the preparation of schiff base?
yes it can be prepared as glucose has an aldehyde group and for preparartion of Schiff base we need a aldehyde or ketone and a primary amine.... glucose can be used as aldehyde.
Is furfaral an acid?
No. It is an aldehyde. Furfural is furan-2-carboxaldehyde.
What happens when timonacic acid is heated?
Timonacic acid is a benign antioxidant that is part of an Aldehyde group. Aldehyde is an organic preservative that breaks down into formaldehyde and releases the chemical into the air when heated.
What is an aldehyde oxidase?
An aldehyde oxidase is an enzyme which catalyzes the oxidation of an aldehyde to a carboxylic acid.
Is formic acid an Aldehyde or a Carboxylic acid?
Formic acid is methanoic acid. A carboxylic acid.
An aldehyde forms a carboxylic acid by?
oxidation
Why glucose is used for the preparation of schiff base?
yes it can be prepared as glucose has an aldehyde group and for preparartion of Schiff base we need a aldehyde or ketone and a primary amine.... glucose can be used as aldehyde.
What is the Cannizzaro reaction?
A Cannizzaro reaction is the disproportionation of an aldehyde into an alcohol and carboxylic acid. The Cannizzaro reaction, named after its discoverer Stanislao Cannizzaro, is a chemical reaction that involves the base-induced disproportionation of two molecules of a non-enolizable aldehyde to give a primary alcohol and a carboxylic acid. Named after: Stanislao Cannizzaro
Is furfaral an acid?
No. It is an aldehyde. Furfural is furan-2-carboxaldehyde.
What happens when timonacic acid is heated?
Timonacic acid is a benign antioxidant that is part of an Aldehyde group. Aldehyde is an organic preservative that breaks down into formaldehyde and releases the chemical into the air when heated.
Is it easier to oxidize an alcohol or an aldehyde?
The oxidation product of an aldehyde will depend on whether the conditions are acidic or alkaline. The aldehyde will oxidize to a carboxylic acid if it is acidic. If it is alkaline, the aldehyde will form a salt because the acid would react.
What products are formed from Synthesis of aldehyde's from acid chlorides?
The easiest way to prepare the aldehyde is the reduction of acid chlorides, the by product is HCl. R-COCl + 2[H] = R-CHO + HCl
What is a Cannizzaro reaction?
A Cannizzaro reaction is the disproportionation of an aldehyde into an alcohol and carboxylic acid.
How do you convert acid to aldehyde directly without converting it to a alcohol?
Pyridinium Chlorochromate
What are all the functional groups that contain a carboxly group?
Acyl bromide (a type of acid halide or acyl halide) Aldehyde Amide Anhydride Carboxylic Acid Enone Ester Ketone
