https://www.sciencemadness.org/smwiki/index.php?title=Ester&feed=atom&action=history
Ester - Revision history
2024-03-29T09:29:15Z
Revision history for this page on the wiki
MediaWiki 1.25.1
https://www.sciencemadness.org/smwiki/index.php?title=Ester&diff=14341&oldid=prev
Mabus: /* Other */
2022-01-02T16:52:34Z
<p><span dir="auto"><span class="autocomment">Other</span></span></p>
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<td colspan='2' style="background-color: white; color:black; text-align: center;">Revision as of 16:52, 2 January 2022</td>
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<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>===Other===</div></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>===Other===</div></td></tr>
<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>Some compounds contain multiple ester groups and are sometimes denoted diesters, triesters, etc. Polyesters are [[<del class="diffchange diffchange-inline">polymers</del>]] that contain esters as part of their main chain.</div></td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>Some compounds contain multiple ester groups and are sometimes denoted diesters, triesters, etc. Polyesters are [[<ins class="diffchange diffchange-inline">polymer</ins>]]<ins class="diffchange diffchange-inline">s </ins>that contain esters as part of their main chain.</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>==Properties==</div></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>==Properties==</div></td></tr>
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Mabus
https://www.sciencemadness.org/smwiki/index.php?title=Ester&diff=6962&oldid=prev
Mabus at 17:09, 27 June 2017
2017-06-27T17:09:53Z
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<td colspan='2' style="background-color: white; color:black; text-align: center;">Revision as of 17:09, 27 June 2017</td>
</tr><tr><td colspan="2" class="diff-lineno" id="L1" >Line 1:</td>
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<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>{{stub}}</div></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>{{stub}}</div></td></tr>
<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>[[File:Methyl formate.png|thumb|220x220px|Methyl formate, the simplest carboxylate ester. The ester functional group is composed of the [[carbonyl]] group, central oxygen, and the carbon of the [[methyl]] group.]]</div></td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>[[File:Methyl formate.png|thumb|220x220px|<ins class="diffchange diffchange-inline">[[</ins>Methyl formate<ins class="diffchange diffchange-inline">]]</ins>, the simplest carboxylate ester. The ester functional group is composed of the [[carbonyl]] group, central oxygen, and the carbon of the [[methyl]] group.]]</div></td></tr>
<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>In organic chemistry, esters are a group of compounds in which the [[hydroxyl]] group of an acid has been replaced by an oxygen atom attached to an [[alkyl]] group<del class="diffchange diffchange-inline">. Organic esters are often centered around a carbon atom that contains a double bond to an oxygen atom, a single bond to another oxygen atom, and a single bond to a carbon atom. They are often derived from a carboxylic acid and an alcohol, such as in [[ethyl acetate]] and [[methyl salicylate]]. Many [[esterification|esterifications]] are very simply done between these components using a dehydrating agent such as [[sulfuric acid]] to drive the reaction</del>.</div></td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>In organic chemistry, <ins class="diffchange diffchange-inline">'''</ins>esters<ins class="diffchange diffchange-inline">''' </ins>are a group of compounds in which the [[hydroxyl]] group of an acid has been replaced by an oxygen atom attached to an [[alkyl]] group.</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del class="diffchange diffchange-inline">The somewhat misleading term "inorganic ester" refers to </del>esters <del class="diffchange diffchange-inline">in which the central oxygen </del>atom <del class="diffchange diffchange-inline">is bound </del>to an atom <del class="diffchange diffchange-inline">other than </del>carbon <del class="diffchange diffchange-inline">that have usually been </del>derived <del class="diffchange diffchange-inline">instead </del>from <del class="diffchange diffchange-inline">an inorganic </del>acid, such as in [[<del class="diffchange diffchange-inline">trimethyl borate</del>]].  </div></td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">==Types==</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">===Organic </ins>esters<ins class="diffchange diffchange-inline">===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">Organic esters are often centered around a carbon </ins>atom <ins class="diffchange diffchange-inline">that contains a double bond </ins>to an <ins class="diffchange diffchange-inline">oxygen </ins>atom<ins class="diffchange diffchange-inline">, a single bond to another oxygen atom, and a single bond to a </ins>carbon <ins class="diffchange diffchange-inline">atom. They are often </ins>derived from <ins class="diffchange diffchange-inline">a [[carboxylic </ins>acid<ins class="diffchange diffchange-inline">]] and an [[alcohol]]</ins>, such as in [[<ins class="diffchange diffchange-inline">ethyl acetate</ins>]] <ins class="diffchange diffchange-inline">and [[methyl salicylate]]. Many [[esterification]]s are very simply done between these components using a dehydrating agent such as [[sulfuric acid]] to drive the reaction</ins>.</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">===Inorganic esters===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">The somewhat misleading term "inorganic ester" refers to esters in which the central oxygen atom is bound to an atom other than carbon that have usually been derived instead from an inorganic acid, usually oxoacids, like [[boric acid]] (ex: [[trimethyl borate]]), [[phosphoric acid]] ([[trimethyl phosphate]]), [[sulfuric acid]] ([[dimethyl sulfate]]), etc. Phosphate esters show good solubility in water, while sulfate esters decompose in water.</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">===Other===</ins></div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>Some compounds contain multiple ester groups and are sometimes denoted diesters, triesters, etc. Polyesters are [[polymers]] that contain esters as part of their main chain.</div></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>Some compounds contain multiple ester groups and are sometimes denoted diesters, triesters, etc. Polyesters are [[polymers]] that contain esters as part of their main chain.</div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">==Properties==</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">Esters are clear colorless liquids, poorly soluble or immiscible with water, but soluble in other organic solvents.</ins></div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>Esters are often characterized by a pleasant fruity or solvent-like odor and a fruity taste, as esters are often the source of the familiar smells and tastes of many fruits and botanical extracts, such as [[Methyl salicylate|wintergreen]]. This leads them to be frequent candidates for fragrances and flavorings.</div></td><td class='diff-marker'> </td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>Esters are often characterized by a pleasant fruity or solvent-like odor and a fruity taste, as esters are often the source of the familiar smells and tastes of many fruits and botanical extracts, such as [[Methyl salicylate|wintergreen]]. This leads them to be frequent candidates for fragrances and flavorings.</div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">==Handling==</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">===Safety===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">Organic esters are flammable.</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">===Storage===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">===Disposal===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">==References==</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"><references/></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">===Relevant Sciencemadness===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
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Mabus
https://www.sciencemadness.org/smwiki/index.php?title=Ester&diff=110&oldid=prev
Zts16: Created page with "{{stub}} Methyl formate, the simplest carboxylate ester. The ester functional group is composed of the [[carbonyl group, central ox..."
2015-06-14T04:00:40Z
<p>Created page with "{{stub}} <a href="/smwiki/index.php/File:Methyl_formate.png" title="File:Methyl formate.png">Methyl formate, the simplest carboxylate ester. The ester functional group is composed of the [[carbonyl</a> group, central ox..."</p>
<p><b>New page</b></p><div>{{stub}}<br />
[[File:Methyl formate.png|thumb|220x220px|Methyl formate, the simplest carboxylate ester. The ester functional group is composed of the [[carbonyl]] group, central oxygen, and the carbon of the [[methyl]] group.]]<br />
In organic chemistry, esters are a group of compounds in which the [[hydroxyl]] group of an acid has been replaced by an oxygen atom attached to an [[alkyl]] group. Organic esters are often centered around a carbon atom that contains a double bond to an oxygen atom, a single bond to another oxygen atom, and a single bond to a carbon atom. They are often derived from a carboxylic acid and an alcohol, such as in [[ethyl acetate]] and [[methyl salicylate]]. Many [[esterification|esterifications]] are very simply done between these components using a dehydrating agent such as [[sulfuric acid]] to drive the reaction.<br />
<br />
The somewhat misleading term "inorganic ester" refers to esters in which the central oxygen atom is bound to an atom other than carbon that have usually been derived instead from an inorganic acid, such as in [[trimethyl borate]]. <br />
<br />
Some compounds contain multiple ester groups and are sometimes denoted diesters, triesters, etc. Polyesters are [[polymers]] that contain esters as part of their main chain.<br />
<br />
Esters are often characterized by a pleasant fruity or solvent-like odor and a fruity taste, as esters are often the source of the familiar smells and tastes of many fruits and botanical extracts, such as [[Methyl salicylate|wintergreen]]. This leads them to be frequent candidates for fragrances and flavorings.<br />
[[Category:Chemical compounds]]<br />
[[Category:Organic compounds]]<br />
[[Category:Types of chemical]]<br />
[[Category:Esters]]<br />
[[Category:Fragrant compounds]]</div>
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