Examples of 'carboxylic acids can' in a sentence
Meaning of "carboxylic acids can"
carboxylic acids can: This phrase suggests that carboxylic acids have the ability or potential to perform certain actions or reactions. It is commonly used in chemistry discussions regarding the properties and reactivity of organic compounds
How to use "carboxylic acids can" in a sentence
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carboxylic acids can
Salts of carboxylic acids can also be used.
Optionally naphthenic acids or synthetic carboxylic acids can be used.
These carboxylic acids can be used alone or in combination.
Trialkylsilylcarboxylates of aliphatic carboxylic acids can be obtained by transesterification.
Carboxylic acids can be made by the oxidation of aldehydes or of alcohols.
Mixtures of olefinic carboxylic acids can also be used.
The carboxylic acids can include stearates and palmitates.
Alkylene and aralkylene carboxylic acids can also be used.
These carboxylic acids can be unsubstituted or substituted as given above.
The cycloaliphatic and aliphatic carboxylic acids can be saturated or unsaturated.
Carboxylic acids can be used as radical precursors in radical fluorination methods.
Mixtures of the derivatives of unsaturated carboxylic acids can also be used.
Unsaturated carboxylic acids can be sulphurized.
The monoesters of fatty acid alkanolamides with carboxylic acids can also be used.
A variety of carboxylic acids can be included.
See also
Monofunctional and / or bifunctional amines and carboxylic acids can be used.
Mixtures of carboxylic acids can be employed in the aforementioned latexes.
Copper oxides and copper salts of organic carboxylic acids can be used as copper compounds.
These carboxylic acids can be used singly or in combination of two or more.
Preferably, low molecular weight carboxylic acids can be used as reaction catalysts.
The carboxylic acids can also be used in their corresponding anhydride form.
Several amino acids and several carboxylic acids can be added according to this method.
The carboxylic acids can comprise linear or branched alkyl groups or aromatic groups.
However, the content of carboxylic acids can be completely unknown.
The carboxylic acids can be saturated or mono - or polyethylenically unsaturated.
For example, both ketones and carboxylic acids can be reduced to alcohols.
The carboxylic acids can be mono - or dibasic.
Di - and trialkyl and alkenyl esters of carboxylic acids can also be used.
The polybasic carboxylic acids can also be used in their functional equivalent form.
The direct oxidation of primary alcohols to carboxylic acids can be carried out using,.
The carboxylic acids can be monoacids, diacids or triacids.
In the presence of a strong acid catalyst, carboxylic acids can condense to form acid anhydrides.
The carboxylic acids can be either straight-chain or branched.
As examples of carboxylic acids comprising a tertiary carbon atom, perfluorinated carboxylic acids can be mentioned.
Acetic acid and other carboxylic acids can be removed with alumina followed by distillation.
However, as discussed below, other companion acids and hydroxy carboxylic acids can be used.
Formulations based on these carboxylic acids can also contain other bactericidal active substances.
Similarly, other a, B-monoethylenically unsaturated anhydrides of carboxylic acids can be employed.
Alternatively, carboxylic acids can be used as solvents.
Carboxylic acids can be converted to thioesters or thioamides using Lawesson 's reagent.
Some structures of suitable heteroaryl carboxylic acids can be found in Figure 2.
Additionally, carboxylic acids can be esterified with alcohols, to produce esters.
Either mono-or poly-functional carboxylic acids can be used.
In general, all carboxylic acids can be ammoxidized to a mixture of nitriles.
Either mono - or poly-functional carboxylic acids can also be used.
In some cases, carboxylic acids can be used as catalysts for the crosslinking reaction.
Carboxylic acids can have one, two, three, or more carboxyl groups.
The suitable aromatic polybasic carboxylic acids can contain for example from 2-36 carbon atoms.
The starting carboxylic acids can be obtained from acetonitrile according to the following reaction diagram,.
After deprotection, the carboxylic acids can be utilized to prepare the compounds of this invention.
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