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Sodium ethoxide

Index Sodium ethoxide

Sodium ethoxide (also is the organic compound with the formula C2H5ONa) is a white to yellowish powder that dissolves in polar solvents such as ethanol. [1]

17 relations: Acetone, Alkoxide, Anhydrous, Base (chemistry), Claisen condensation, Enol, Ethanol, Hygroscopy, Malonic ester synthesis, Methanol, Miscibility, Nucleophilic substitution, Organic compound, Precipitation (chemistry), Salt metathesis reaction, Sodium, Transesterification.

Acetone

Acetone (systematically named propanone) is the organic compound with the formula (CH3)2CO.

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Alkoxide

An alkoxide is the conjugate base of an alcohol and therefore consists of an organic group bonded to a negatively charged oxygen atom.

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Anhydrous

A substance is anhydrous if it contains no water.

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Base (chemistry)

In chemistry, bases are substances that, in aqueous solution, release hydroxide (OH−) ions, are slippery to the touch, can taste bitter if an alkali, change the color of indicators (e.g., turn red litmus paper blue), react with acids to form salts, promote certain chemical reactions (base catalysis), accept protons from any proton donor, and/or contain completely or partially displaceable OH− ions.

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Claisen condensation

The Claisen condensation is a carbon–carbon bond forming reaction that occurs between two esters or one ester and another carbonyl compound in the presence of a strong base, resulting in a β-keto ester or a β-diketone.

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Enol

Enols, or more formally, alkenols, are a type of reactive structure or intermediate in organic chemistry that is represented as an alkene (olefin) with a hydroxyl group attached to one end of the alkene double bond.

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Ethanol

Ethanol, also called alcohol, ethyl alcohol, grain alcohol, and drinking alcohol, is a chemical compound, a simple alcohol with the chemical formula.

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Hygroscopy

Hygroscopy is the phenomenon of attracting and holding water molecules from the surrounding environment, which is usually at normal or room temperature.

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Malonic ester synthesis

The malonic ester synthesis is a chemical reaction where diethyl malonate or another ester of malonic acid is alkylated at the carbon alpha (directly adjacent) to both carbonyl groups, and then converted to a substituted acetic acid.

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Methanol

Methanol, also known as methyl alcohol among others, is a chemical with the formula CH3OH (a methyl group linked to a hydroxyl group, often abbreviated MeOH).

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Miscibility

Miscibility is the property of substances to mix in all proportions (that is, to fully dissolve in each other at any concentration), forming a homogeneous solution.

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Nucleophilic substitution

In organic and inorganic chemistry, nucleophilic substitution is a fundamental class of reactions in which an electron rich nucleophile selectively bonds with or attacks the positive or partially positive charge of an atom or a group of atoms to replace a leaving group; the positive or partially positive atom is referred to as an electrophile.

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Organic compound

In chemistry, an organic compound is generally any chemical compound that contains carbon.

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Precipitation (chemistry)

Precipitation is the creation of a solid from a solution.

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Salt metathesis reaction

A salt metathesis reaction (from the Greek μετάθεσις, "transposition"), sometimes called a double replacement reaction or double displacement reaction, is a chemical process involving the exchange of bonds between two reacting chemical species, which results in the creation of products with similar or identical bonding affiliations.

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Sodium

Sodium is a chemical element with symbol Na (from Latin natrium) and atomic number 11.

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Transesterification

In organic chemistry, transesterfication is the process of exchanging the organic group R″ of an ester with the organic group R′ of an alcohol.

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Redirects here:

C2H5ONa, CH3CH2ONa, Caustic alcohol, NaC2H5O, NaOCH2CH3, NaOEt, Sodium ethylate.

References

[1] https://en.wikipedia.org/wiki/Sodium_ethoxide

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