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The synthesis of vitamin C begin with glucose !

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What is the role of the mineral acids in the esterification process?

Mineral acids, like sulfuric acid, are used in esterification to catalyze the reaction between an alcohol and a carboxylic acid to form an ester. They protonate the carbonyl group in the carboxylic acid, making it more reactive towards the alcohol. This protonation leads to the formation of an intermediate that eventually rearranges to form the ester.


How can one determine the appropriate name for an ester compound?

To determine the appropriate name for an ester compound, one must identify the parent carboxylic acid and alcohol molecules that make up the ester. The name of the ester is typically derived from the alcohol portion first, followed by the carboxylic acid portion with the ending "-ate." The naming convention follows the format: alkyl group from alcohol -yl name of carboxylic acid -ate.


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.


What conditions are needed to make esters?

They vary - but nearly always involve reflux followed by removal of water often with the aid of an azeotropic solvent. An acid catalyst such as concentrated sulfuric acid is often employed but titanates and other catalysts have also been used.


What alcohol makes propyl ethonate has the formula CH3CH2CH2OH?

Propyl ethanoate is made from propanol (CH3CH2CH2OH) and ethanoic acid (CH3COOH) through an esterification reaction, which involves the combination of an alcohol and carboxylic acid in the presence of an acid catalyst.


Will you add carboxylic acid to make carboxylate salt?

Yes, carboxylic acids can be converted into carboxylate salts by reacting them with a base. The base will deprotonate the carboxylic acid, resulting in the formation of a carboxylate salt and water.


Which groups make up amino acid?

Carboxylic group + Amino group


What are the advantages of carboxylic acid?

Carboxylic acids are versatile compounds with various uses including in the food industry as preservatives and flavor enhancers, in the pharmaceutical industry as drug intermediates, and in the production of plastics and polymers. They also play a crucial role in biochemistry as key components of fatty acids and amino acids. Additionally, carboxylic acids can participate in a variety of chemical reactions due to the reactivity of their functional group.


What reactants are needed to make ester methyl butanoate?

To make methyl butanoate, you would need methanol (CH3OH) and butanoic acid (C4H8O2) as the reactants. The reaction would be a condensation reaction between an alcohol (methanol) and a carboxylic acid (butanoic acid) catalyzed by an acid catalyst, such as sulfuric acid.


What professionals need to use carboxylic acid in their practices?

The chemical carboxylic acid is used by some chemists to make up medicines and creams to give to their patients. Some doctors will use it for their patients as well.


How can you make hydrocarbon?

A hydrocarbon such as an alkane can be made from a Kolbe electrolysis of the sodium salt of the carboxylic acid.


What elements make up lactic acid?

Lactic acid is composed of carbon, hydrogen, and oxygen atoms. It is a carboxylic acid with the chemical formula C3H6O3.