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・ Carboximidate
・ Carboxy-cis,cis-muconate cyclase
・ Carboxy-lyases
・ Carboxyamidotriazole
・ Carboxybenzyl
・ Carboxybiotin decarboxylase
・ Carboxycyclophosphamide
・ Carboxydocella thermautotrophica
・ Carboxydothermus hydrogenoformans
・ Carboxyfluorescein
・ Carboxyfluorescein diacetate succinimidyl ester
・ Carboxyfluorescein succinimidyl ester
・ Carboxyglutamic acid
・ Carboxyhemoglobin
・ Carboxyl transferase domain
Carboxylate
・ Carboxylate reductase
・ Carboxylate transporter
・ Carboxylation
・ Carboxylesterase
・ Carboxylesterase 1
・ Carboxylesterase 2
・ Carboxylesterase 3
・ Carboxylesterase family
・ Carboxylic acid
・ Carboxymethyl cellulose
・ Carboxymethylenebutenolidase
・ Carboxymethylhydantoinase
・ Carboxymethyloxysuccinate lyase
・ Carboxynorspermidine decarboxylase


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Carboxylate : ウィキペディア英語版
Carboxylate

A carboxylate is a salt or ester of a carboxylic acid.
''Carboxylate salts'' have the general formula M(RCOO)''n'', where M is a metal and ''n'' is 1,2,...; ''carboxylate esters'' have the general formula RCOOR'. R and R' are organic groups; R'≠H.
A carboxylate ion is the conjugate base of a carboxylic acid, RCOO. It is an ion with negative charge.
== Resonance stabilization of the carboxylate ion==
Carboxylic acids easily dissociate into a carboxylate anion and a positively charged hydrogen ion (proton), much more readily than alcohols do (into an alkoxide ion and a proton), because the carboxylate ion is stabilized by resonance. The negative charge that is left after deprotonation of the carboxyl group is delocalized between the two electronegative oxygen atoms in a resonance structure.
:
This delocalization of the electron cloud means that both of the oxygen atoms are less strongly negatively charged; the positive proton is therefore less strongly attracted back to the carboxylate group once it has left; the carboxylate ion is more stable . In contrast, an alkoxide ion, once formed, would have a strong negative charge on the oxygen atom, which would make it difficult for the proton to escape. Carboxylic acids have a lower pH than alcohols: the higher the number of protons in solution, the lower the pH.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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