https://www.conservapedia.com/index.php?action=history&feed=atom&title=Acyl_halide 2026-09-26T09:59:04Z Revision history for this page on the wiki MediaWiki 1.35.14 https://www.conservapedia.com/index.php?title=Acyl_halide&diff=720109&oldid=prev 2009-11-14T20:36:38Z

<p>cat</p> <table class="diff diff-contentalign-left diff-editfont-monospace" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:36, November 14, 2009</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l2" >Line 2:</td> <td colspan="2" class="diff-lineno">Line 2:</td></tr> <tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr> <tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>Acyl chlorides can be reacted with [[alcohol]] in order to produce an [[ester]] and an acid. This reaction provides a better yield than the alternative; reacting a carboxylic acid and an alcohol.</div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>Acyl chlorides can be reacted with [[alcohol]] in order to produce an [[ester]] and an acid. This reaction provides a better yield than the alternative; reacting a carboxylic acid and an alcohol.</div></td></tr> <tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="color: #202122; 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: #202122; 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;">[[Category:Organic Chemistry]]</ins></div></td></tr> </table>

OscarJ https://www.conservapedia.com/index.php?title=Acyl_halide&diff=719093&oldid=prev 2009-11-11T21:29:05Z

<p></p> <table class="diff diff-contentalign-left diff-editfont-monospace" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 21:29, November 11, 2009</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l1" >Line 1:</td> <td colspan="2" class="diff-lineno">Line 1:</td></tr> <tr><td class='diff-marker'>−</td><td style="color: #202122; 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>An '''acyl halide''', alternatively known as an '''acid halide''' is an organic compound consisting of the functional group RCOX, where R is a hydrocarbon chain and X is a halide, such as chlorine, bromine or iodine. They can be produced from a [[carboxylic]] <del class="diffchange diffchange-inline">acid </del>by reacting it with a compound such as phosphorous trichloride (for chlorides) or phosphorous pentabromide (for bromides).</div></td><td class='diff-marker'>+</td><td style="color: #202122; 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>An '''acyl halide''', alternatively known as an '''acid halide''' is an organic compound consisting of the functional group RCOX, where R is a hydrocarbon chain and X is a halide, such as chlorine, bromine or iodine. They can be produced from a [[carboxylic <ins class="diffchange diffchange-inline">acid</ins>]] by reacting it with a compound such as phosphorous trichloride (for chlorides) or phosphorous pentabromide (for bromides).</div></td></tr> <tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr> <tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>Acyl chlorides can be reacted with [[alcohol]] in order to produce an [[ester]] and an acid. This reaction provides a better yield than the alternative; reacting a carboxylic acid and an alcohol.</div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>Acyl chlorides can be reacted with [[alcohol]] in order to produce an [[ester]] and an acid. This reaction provides a better yield than the alternative; reacting a carboxylic acid and an alcohol.</div></td></tr> </table>

GideonFox https://www.conservapedia.com/index.php?title=Acyl_halide&diff=719092&oldid=prev 2009-11-11T21:28:40Z

<p>Created page with &#039;An &#039;&#039;&#039;acyl halide&#039;&#039;&#039;, alternatively known as an &#039;&#039;&#039;acid halide&#039;&#039;&#039; is an organic compound consisting of the functional group RCOX, where R is a hydrocarbon chain and X is a halide...&#039;</p> <p><b>New page</b></p><div>An '''acyl halide''', alternatively known as an '''acid halide''' is an organic compound consisting of the functional group RCOX, where R is a hydrocarbon chain and X is a halide, such as chlorine, bromine or iodine. They can be produced from a [[carboxylic]] acid by reacting it with a compound such as phosphorous trichloride (for chlorides) or phosphorous pentabromide (for bromides).<br /> <br /> Acyl chlorides can be reacted with [[alcohol]] in order to produce an [[ester]] and an acid. This reaction provides a better yield than the alternative; reacting a carboxylic acid and an alcohol.</div>

GideonFox