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synthesis$81233$ - traduzione in greco
CHEMICAL REACTION
Wohler synthesis; Woehler synthesis
synthesis
n. σύνθεση
ethyl alcohol
![[[Near-infrared spectrum]] of liquid ethanol](https://commons.wikimedia.org/wiki/Special:FilePath/Ethanol near IR spectrum.png?width=200 "[[Near-infrared spectrum]] of liquid ethanol")
![USP grade]] ethanol for laboratory use](https://commons.wikimedia.org/wiki/Special:FilePath/Ethyl alcohol usp grade.jpg?width=200 "USP grade]] ethanol for laboratory use")
CHEMICAL COMPOUND
CH3CH2OH; C2H5OH; Ethyl alcohol; Absolute alcohol; Grain alcohol; EtOH; Hydration of ethene; Ethyl Alcohol; Ethanol-alcohol; Bioethanol; Bio-ethanol; Ethylalcohol; Hydroxyethane; Anhydrous ethanol; Hydrous ethanol; Absolute ethanol; E1510; Industrial alcohol; Industrial ethanol; Etanol; Chemical derivatives of ethanol; Ethanol purification; Wine spirit; Ethyl alchohol; C2h50h; Ethonal; Ethonol; Wet alcohol; Ethyl hydrate; Pure alcohol; Hydroxyethyl; Ethyloxidane; Drying ethanol; C₂H₅OH; ATC code D08AX08; ATCvet code QD08AX08; ATC code V03AB16; ATCvet code QV03AB16; ATC code V03AZ01; ATCvet code QV03AZ01; Aethanol; Aethylalkohol; Algrain; Anhydrol; Denatured Alcohol Cd-10; Denatured Alcohol Cd-5; Denatured Alcohol Cd-5a; Denatured Alcohol Sd-1; Denatured Alcohol Sd-13a; Denatured Alcohol Sd-17; Denatured Alcohol Sd-23a; Denatured Alcohol Sd-28; Denatured Alcohol Sd-30; Denatured Alcohol Sd-39b; Denatured Alcohol Sd-39c; Denatured Alcohol Sd-3a; Denatured Alcohol Sd-40m; Ethanol, Silent Spirit; Reagent Alcohol; Synasol; Thanol; Thiofaco M-50; Ethylic alcohol; Bio ethanol; Anhydrous alcohol; Ethanolic; Methylcarbinol; Ethylol; Ehtanol; Cologne spirit; Endogenous ethanol; Endogenous ethanol in humans; Acquarzente; Cologne spirits; Synthesis of ethanol; Water-alcohol; Methyl carbinol; History of ethanol; Potable alcohol
αιθυλικό οινόπνευμα
absolute alcohol
CHEMICAL COMPOUND
CH3CH2OH; C2H5OH; Ethyl alcohol; Absolute alcohol; Grain alcohol; EtOH; Hydration of ethene; Ethyl Alcohol; Ethanol-alcohol; Bioethanol; Bio-ethanol; Ethylalcohol; Hydroxyethane; Anhydrous ethanol; Hydrous ethanol; Absolute ethanol; E1510; Industrial alcohol; Industrial ethanol; Etanol; Chemical derivatives of ethanol; Ethanol purification; Wine spirit; Ethyl alchohol; C2h50h; Ethonal; Ethonol; Wet alcohol; Ethyl hydrate; Pure alcohol; Hydroxyethyl; Ethyloxidane; Drying ethanol; C₂H₅OH; ATC code D08AX08; ATCvet code QD08AX08; ATC code V03AB16; ATCvet code QV03AB16; ATC code V03AZ01; ATCvet code QV03AZ01; Aethanol; Aethylalkohol; Algrain; Anhydrol; Denatured Alcohol Cd-10; Denatured Alcohol Cd-5; Denatured Alcohol Cd-5a; Denatured Alcohol Sd-1; Denatured Alcohol Sd-13a; Denatured Alcohol Sd-17; Denatured Alcohol Sd-23a; Denatured Alcohol Sd-28; Denatured Alcohol Sd-30; Denatured Alcohol Sd-39b; Denatured Alcohol Sd-39c; Denatured Alcohol Sd-3a; Denatured Alcohol Sd-40m; Ethanol, Silent Spirit; Reagent Alcohol; Synasol; Thanol; Thiofaco M-50; Ethylic alcohol; Bio ethanol; Anhydrous alcohol; Ethanolic; Methylcarbinol; Ethylol; Ehtanol; Cologne spirit; Endogenous ethanol; Endogenous ethanol in humans; Acquarzente; Cologne spirits; Synthesis of ethanol; Water-alcohol; Methyl carbinol; History of ethanol; Potable alcohol
καθαρό οινόπνευμα
Definizione
synthesize
(synthesizes, synthesizing, synthesized)
Note: in BRIT, also use 'synthesise'
1.
To synthesize a substance means to produce it by means of chemical or biological reactions. (TECHNICAL)
After extensive research, Albert Hoffman first succeeded in synthesizing the acid in 1938...
VERB: V n
2.
If you synthesize different ideas, facts, or experiences, you combine them to form a single idea or impression. (FORMAL)
The movement synthesised elements of modern art that hadn't been brought together before, such as Cubism and Surrealism.
= fuse
VERB: V n
Wikipedia
Wöhler synthesis
The Wöhler synthesis is the conversion of ammonium cyanate into urea. This chemical reaction was described in 1828 by Friedrich Wöhler. It is often cited as the starting point of modern organic chemistry. Although the Wöhler reaction concerns the conversion of ammonium cyanate, this salt appears only as an (unstable) intermediate. Wöhler demonstrated the reaction in his original publication with different sets of reactants: a combination of cyanic acid and ammonia, a combination of silver cyanate and ammonium chloride, a combination of lead cyanate and ammonia and finally from a combination of mercury cyanate and cyanatic ammonia (which is again cyanic acid with ammonia).
