Examples of 'ethers can' in a sentence

Meaning of "ethers can"

ethers can: This phrase refers to the idea that utilizing ethers, which are a class of organic compounds, can have various effects or outcomes. For instance, 'In the experiment, the researchers discovered that ethers can act as effective solvents.'

How to use "ethers can" in a sentence

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ethers can
The ethers can be used as gasoline components.
A wide array of glycol ethers can be used.
Ethers can also be used as solvent.
Mixtures of glycol ethers can be used as suspending agents.
Yet additionally, hydrophobically modified cellulose ethers can be used.
Cellulose ethers can be mentioned as suitable water retentive agents.
A mixture of two vinyl ethers can also be used.
One or more ethers can be comprised in the stabilizer composition.
Exchanges can be hacked and your ethers can be stolen.
The glycidyl ethers can be preextended with diols or may be prepolymers.
There are many other ways in which polybromodiphenyl ethers can be modified in the environment.
These vinyl ethers can be produced by any of the conventional methods.
Other than these, dibenzocrown ethers can be also mentioned.
Glycidol ethers can also be prepared by following the procedures described below.
Chenodeoxycholate or polyoxyethylene ethers can be used in place of the deoxycholate.

See also

Starch ethers can also be formed for use in the present invention.
In some embodiments, the polyalkylene glycol ethers can be represented by the formula,.
Cellulose ethers can be modified by attaching different substituents to hydroxyl groups in cellulose.
According to the invention, a mixture of different polyoxyalkylene diglycidyl ethers can be used as well.
The functionalized vinyl ethers can be obtained in a conventional manner.
The ethers can be selected from dimethyl ether, diethyl ether, dimethoxymethane or dipropoxymethane.
Copolymers obtained by grafting styrene-based compounds to such polyphenylene ethers can also be used.
These monoalkylglyceryl ethers can be used alone or as optional mixtures.
In view of the above-mentioned conditions, some of alcohols and ethers can be used preferentially.
The various silyl ethers can be removed by reaction with tetrabutylammonium fluoride.
Esters are preferred, but carbonates, urethanes and especially ethers can also advantageously be used.
It is believed that such ethers can cause catalyst deactivation by adsorption onto the catalyst.
By choosing various etherification agents for the reaction, various cellulose ethers can be obtained efficiently.
Cellulose ethers can alter the viscosity or other rheological characteristics of liquid detergent products.
The physical data for these glycidyl ethers can be seen from Table 2.
Ethylenic ethers can likewise fix RF I under the operating conditions described.
Non-limiting examples of suitable acyclic polyvinyl ethers can include those represented by the following formula X,.
Indazolyl ethers can be prepared by the process outlined in Scheme 9.
Dialkylphenacyl - sulfonium salts, hexafluorophosphate, alpha-sulfonyloxy ketone, and silyl benzyl ethers can be used as well.
The bisglycidyl ethers can be aromatic, aliphatic or cycloaliphatic.
By way of example, aromatic, cycloaliphatic and / or aliphatic ethers can be contemplated as ethers C5.
Surprisingly n, n ethers can be formed by dehydration of n - alcohols with little or no rearrangement.
The various vinyl ethers can be represented by the formula,.
Illustrative vinyl ethers can include triethyleneglycol divinyl ether, divinyl ether, or any mixture thereof.
For example, the use of ethers can reduce the stereospecificity of the catalyst.
Glycols and glycol ethers can also be added as solvents, plasticizers or diluents.
Some esters, ketones and ethers can be employed for plasticizing a nitrocellulose varnish.
Scheme 16 describes how ethers can be synthesized from analogs and derivatives of adenine.
Typically, alkylvinyl ethers can be acylated with haloakylacetic anhydrides to yield compounds of type II.
The resulting silyl ethers can be hydrolyzed with 1 M hydrochloric acid.
Monofunctional terminated polyphenyl ethers can be prepared according to procedures described in literature J. Org.
Heck reaction with vinyl ethers can introduce a keto-group, which can be subsequently functionalized ( method 5 ).
The cyclic ethers can be represented by Formula 1, where.
All of these aminoaryl ethers can subsequently be incorporated into amides of formulae ( I-IV ).
Among the preferred allyl ethers can be cited the compounds of formula, STR3.

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