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An organic molecule with the functional group O=C−O. This is also known as an ester.

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How does the size of the alkyl group in an alcohol affect the vigor of its reaction with sodium metal?

The larger the alkyl group, the less energeticthe reaction, because the hydroxyl groups are "diluted". byadding more alkyl groups, you decrease the concentrationof hydroxyl groups and therefore make the molecule less polar. thisdecreases the vigor of reaction with sodium metal.


What happens when Alkyl halide reacts with silver nitrate?

When an alkyl halide reacts with silver nitrate, a substitution reaction takes place where the halide ion is displaced by the silver ion to form a silver halide precipitate. The alkyl group remains unchanged in the reaction.


How many distinct alkene products are possible when a alkyl halide undergoes E2 elimination?

Two distinct alkene products are possible when an alkyl halide undergoes E2 elimination. One product results from the removal of a beta hydrogen on one side of the molecule, while the other product results from the removal of a beta hydrogen on the opposite side.


What is alkyl calcium carbamate used for?

Alkyl calcium carbamate is used as a processing aid and vulcanizing agent in the rubber industry. It helps to improve the curing process of rubber compounds, enhancing their mechanical properties and overall performance.


Are alkyl nitrate poppers stimulants or hallucinogens?

Alkyl nitrate poppers are classified as stimulants due to their vasodilatory effects, which lead to increased heart rate and blood flow. They do not cause hallucinations like traditional hallucinogens.

Related Questions

What is an alkanoate?

An alkanoate is a type of organic compound that contains a carboxylate group –COO attached to an alkyl chain. It is commonly found in esters, which are formed by the reaction between a carboxylic acid and an alcohol. Alkanoates are widely used in the production of chemicals, flavorings, and fragrances.


What is the suffix for alkyl groups?

The suffix for alkyl groups is -yl.


What are other examples of alkyl halide?

an example of Alkyl halides is R-X ( x represents any halogen) C2F4 is Teflon it is an example of Alkyl Halides


Which is the contaminant soap alkyl benzene sulfonate or linear alkyl sulfonate?

Depending on the desired definition of the word "contaminant" Alkyl Benzene Sulfonate is more likely the answer. Linear Alkyl Sulfonates are far more readily biodegraded than Alkyl Benzene Sulfonate due to their relative chemical structures. Alkyl Benzene Sulfonate can cause issues in waterways such as eutrophication, which in turn can lead to algal blooms.


What is the name of the alkyl group -C4H9?

Butyl! Alkane is CnH2n+2 Alkyl group is alkane - hydrogen CnH2n+1


What is the name for the CH3-Ch-CH3 alkyl group?

The name for the CH3-Ch-CH3 alkyl group is isopropyl.


What is an alkyl nitrite?

An alkyl nitrite is any of a class of inhalant recreational drugs, originally developed for the treatment of angina.


What alkyl group is attached to the oxygen in the following ester?

The alkyl group attached to the oxygen in the ester is the R group.


What is a lower alkyl?

A lower alkyl refers to a simple alkyl group with a smaller number of carbon atoms, such as methyl (CH3) and ethyl (C2H5). These alkyl groups are often found as substituents in organic compounds and play important roles in chemical reactions and biological processes.


What is an alkyl phosphate?

An alkyl phosphate is a chemical compound consisting of a phosphate group bonded to an alkyl group. These compounds are widely used in various applications, including as surfactants in cleaning products and as flame retardants in plastics.


What is structure of alkyl isocyanide?

Alkyl isocyanides have the general formula R-N≡C, where R is an alkyl group. The isocyanide functional group consists of a carbon atom triple-bonded to a nitrogen atom. Alkyl isocyanides are known for their pungent, disagreeable odors.


Why tertiary alkyl radical more stable than primary?

Tertiary alkyl radicals are more stable than primary alkyl radicals because they have more hyperconjugation interactions with adjacent carbon-hydrogen bonds that can delocalize the radical's charge, stabilizing it. In addition, tertiary alkyl radicals are surrounded by more alkyl groups, which provide steric hindrance and shield the radical from reacting with other molecules.