In zeisel method for the determination of methoxy group?

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A method of determining the number of methoxy (–OCH3) groups in an organic compound. The compound is heated wih excess hydriodic acid, forming an alcohol and iodomethane:R-O-CH3+HI → ROH+CH3I The iodomethane is distilled off and led into an alcoholic solution of silver nitrate, where it precipitates silver iodide.

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In this regard, What is Zeisel method?

Zeisel's method is a method for the determination of methoxyl and ethoxyl grouos in organic compounds,in which the substance is heated with hydriodic acid,thw iodoalkane thus formed is passed into an ethanolic solution of silver I nitrate,and the resulting silver I iodide weighed.

Herein, Which method is used for the estimation of a methoxy group in organic compounds?. Gas-liquid chromatography combined with hydriodic acid digestion has been used to determine methoxy groups in soil.

Then, Which group is detected and estimated quantitatively by Zeisel method?

The alkoxyl group such as methoxy (–OCH3), ethoxy (–OC2H5) occur in alkaloids which are detected and estimated by Zeisel method.

How do you test for ethers?

The Zeisel determination or Zeisel test is a chemical test for the presence of esters or ethers in a chemical substance. It is named after the Czech chemist Simon Zeisel (1854–1933). In a qualitative test a sample is first reacted with a mixture of acetic acid and hydrogen iodide in a test tube.

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What are the uses of ethers?

They are relatively unreactive, and as a result they are useful as solvents for fats, oils, waxes, perfumes, resins, dyes, gums, and hydrocarbons. Vapours of certain ethers are used as insecticides, miticides, and fumigants for soil.

What is the test for aldehydes?

The Tollens' test is a reaction that is used to distinguish aldehydes from ketones, as aldehydes are able to be oxidized into a carboxylic acid while ketones cannot. Tollens' reagent, which is a mixture of silver nitrate and ammonia, oxidizes the aldehyde to a carboxylic acid.

How do you test for esters?

A simple way of detecting the smell of the ester is to pour the mixture into some water in a small beaker. Apart from the very small ones, esters are fairly insoluble in water and tend to form a thin layer on the surface. Excess acid and alcohol both dissolve and are tucked safely away under the ester layer.

What is ethers what is methods of preparation of ethers?

Williamson's synthesis is an important method for the preparation of symmetrical and asymmetrical ethers in laboratories. In this method, an alkyl halide is reacted with sodium alkoxide which leads to the formation of ether. The reaction generally follows the SN2 mechanism for primary alcohol.

What is OMe in organic chemistry?

The methoxy group is the simplest alkoxy group. The methoxy group is commonly abbreviated -OMe in reactions.

How do ethers react with hi?

Alkyl ethers are cleaved by the strong acids HI or HBr in a nucleophilic substitution reaction similar to that of alcohols. Protonation of the ethereal oxygen creates a good leaving group, a neutral alcohol molecule. The halide ion, bromide or iodide are both good nucleophiles.

Is used to determine the number of methoxy groups in alkaloids?

As we know that the Zeisel's method is used to count the number of methoxy groups in that compound.

Which method is used to determine the number of methoxy groups in alkaloids?

A method of determining the number of methoxy (–OCH3) groups in an organic compound. The compound is heated wih excess hydriodic acid, forming an alcohol and iodomethane:R-O-CH3+HI → ROH+CH3I The iodomethane is distilled off and led into an alcoholic solution of silver nitrate, where it precipitates silver iodide.

What is Williamson ether synthesis used for?

The Williamson ether synthesis is the most widely used method to produce ethers. It occurs by an SN2 reaction in which a metal alkoxide displaces a halide ion from an alkyl halide. The alkoxide ion is prepared by the reaction of an alcohol with a strong base such as sodium hydride.

How ethers are formed?

Bimolecular dehydration

In the presence of acid, two molecules of an alcohol may lose water to form an ether. In practice, however, this bimolecular dehydration to form an ether competes with unimolecular dehydration to give an alkene. ... Dehydration is used commercially to produce diethyl ether.

How is anisole prepared?

Preparation. Anisole is prepared by methylation of sodium phenoxide with dimethyl sulfate or methyl chloride: 2 C6H5ONa+ + (CH3O)2SO2 → 2 C6H5OCH3 + Na2SO.

How do you synthesis ethers?

There are two primary reactions to generate ethers: either by Dehydration of Alcohols or by the Williamson Synthesis. Acyclic ethers can be prepared using Williamson's synthesis, which involves reacting an alkoxide with a haloalkane.

What is ester formula?

Carboxylic acid esters, formula RCOOR′ (R and R′ are any organic combining groups), are commonly prepared by reaction of carboxylic acids and alcohols in the presence of hydrochloric acid or sulfuric acid, a process called esterification.

Are esters acidic or basic?

Esters are neutral compounds, unlike the acids from which they are formed. In typical reactions, the alkoxy (OR′) group of an ester is replaced by another group. One such reaction is hydrolysis, literally “splitting with water.” The hydrolysis of esters is catalyzed by either an acid or a base.

What is esterification give an example?

Some esters can be prepared by esterification, a reaction in which a carboxylic acid and an alcohol, heated in the presence of a mineral acid catalyst, form an ester and water: The reaction is reversible. As a specific example of an esterification reaction, butyl acetate can be made from acetic acid and 1-butanol.

What does Schiff's test for?

The Schiff test is a chemical test used to check the presence of aldehydes in a solution. This is done by reacting the solution with a small quantity of Schiff's reagent. Schiff's reagent is the reaction product of a dye such as fuchsin and sodium bisulfite.

What is the 2/4 DNP test?

The 2,4-DNP test is a tried and true method for the presence of aldehyde and ketone functional groups in unknown organic compounds. When an aldehyde or a ketone is placed in a 2,4-DNP solution, a bright yellow-orange or red solid results, which constitutes a positive test.

Is aldehyde acidic or basic?

The gas-phase acidity of aldehyde was found to be 1,640 kJ/mol (393 kcal/mol), making it more acidic than hydrogen (1,700 kJ/mol, 400 kcal/mol) and ammonia (1,680 kJ/mol, 402 kcal/mol), but less acidic than water (1,600 kJ/mol, 390 kcal/mol) in the gas phase.

What are the two uses of esters?

There are various uses of esters.
  • Esters that are have fragrant odours are used as a constituent of perfumes, essential oils, food flavourings, cosmetics, etc.
  • Esters are used as an organic solvent.
  • Natural esters are found in pheromones.
  • Naturally occurring fats and oils are fatty acid esters of glycerol.

What products contain ethers?

Endless Uses for Glycol Ethers
  • Brake fluids.
  • Coating.
  • Compounders.
  • Cosmetics.
  • Dyes.
  • Engraving.
  • Gypsum.
  • Lacquers.