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	<title>Chemisrty &#187; concentration</title>
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	<description>chemistry,inorganical,analitical,chemistry,biochemistry,polymer,organic chemistry,chemist,chem,chemican,amino acids,acid,bases,titration,carbohydrate,lipid,thermodynamics,chemical video,education,atom,ions,laboratory</description>
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		<title>Le Chatelier&#8217;s Principle</title>
		<link>http://www.kimyaturk.org/le-chateliers-principle/</link>
		<comments>http://www.kimyaturk.org/le-chateliers-principle/#comments</comments>
		<pubDate>Wed, 08 Sep 2010 10:13:20 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Physical Chemistry]]></category>
		<category><![CDATA[chemical equilibrium]]></category>
		<category><![CDATA[chemical reaction]]></category>
		<category><![CDATA[chemist]]></category>
		<category><![CDATA[chemists]]></category>
		<category><![CDATA[concentration]]></category>
		<category><![CDATA[disciplines]]></category>
		<category><![CDATA[economic equilibrium]]></category>
		<category><![CDATA[henry louis le chatelier]]></category>
		<category><![CDATA[homeostasis]]></category>
		<category><![CDATA[karl ferdinand braun]]></category>
		<category><![CDATA[lenz]]></category>
		<category><![CDATA[partial pressure]]></category>
		<category><![CDATA[principle]]></category>

		<guid isPermaLink="false">http://www.kimyaturk.org/?p=1101</guid>
		<description><![CDATA[Learn what Le Chatelier&#8217;s Principle is and how it can be applied to predict the effect of a change in conditions on chemical equilibrium. What Is Le Chatelier&#8217;s Principle? Le Chatelier&#8217;s Principle is the name given to the principle in which a change in a chemical system prompts an opposing reaction. In chemistry, this principle [...]]]></description>
			<content:encoded><![CDATA[<p>Learn what Le Chatelier&#8217;s Principle is and how it can be applied to predict the effect of a change in conditions on <a href="http://www.kimyaturk.org/tag/chemical-equilibrium/" class="st_tag internal_tag" rel="tag" title="Posts tagged with chemical equilibrium">chemical equilibrium</a>.</p>
<h3>What Is Le Chatelier&#8217;s Principle?</h3>
<p>Le Chatelier&#8217;s Principle is the name given to the principle in which a change in a chemical system prompts an opposing reaction. In chemistry, this principle was discovered independently by <a href="http://www.kimyaturk.org/tag/henry-louis-le-chatelier/" class="st_tag internal_tag" rel="tag" title="Posts tagged with henry louis le chatelier">Henry Louis Le Chatelier</a> and <a href="http://www.kimyaturk.org/tag/karl-ferdinand-braun/" class="st_tag internal_tag" rel="tag" title="Posts tagged with karl ferdinand braun">Karl Ferdinand Braun</a>, so it is sometimes called the Le Chatelier-Braun Principle. The principle can be stated as follows:</p>
<p>If the temperature, <a href="http://www.kimyaturk.org/tag/concentration/" class="st_tag internal_tag" rel="tag" title="Posts tagged with concentration">concentration</a>, volume, or <a href="http://www.kimyaturk.org/tag/partial-pressure/" class="st_tag internal_tag" rel="tag" title="Posts tagged with partial pressure">partial pressure</a> of a chemical system at <a href="http://www.kimyaturk.org/tag/equilibrium/" class="st_tag internal_tag" rel="tag" title="Posts tagged with equilibrium">equilibrium</a> changes, then the <a href="http://www.kimyaturk.org/tag/equilibrium/" class="st_tag internal_tag" rel="tag" title="Posts tagged with equilibrium">equilibrium</a> shifts to compensate for the change.</p>
<p>The more general form of the principle applies to other <a href="http://www.kimyaturk.org/tag/disciplines/" class="st_tag internal_tag" rel="tag" title="Posts tagged with disciplines">disciplines</a>. Homeostasis and Lenz&#8217;s law are examples. Le Chatelier&#8217;s Principle is known by the same name when applied to <a href="http://www.kimyaturk.org/tag/economic-equilibrium/" class="st_tag internal_tag" rel="tag" title="Posts tagged with economic equilibrium">economic equilibrium</a>.</p>
<h3>How Is Le Chatelier&#8217;s Principle Used?</h3>
<p>Le Chatelier&#8217;s Principle is used to predict how a change in pressure, volume, concentration, or temperature will affect chemical equilibrium. Knowing the impact on equilibrium allows <a href="http://www.kimyaturk.org/tag/chemists/" class="st_tag internal_tag" rel="tag" title="Posts tagged with chemists">chemists</a> to manipulate the <a href="http://www.kimyaturk.org/tag/chemical-reaction/" class="st_tag internal_tag" rel="tag" title="Posts tagged with chemical reaction">chemical reaction</a>. For example, a <a href="http://www.kimyaturk.org/tag/chemist/" class="st_tag internal_tag" rel="tag" title="Posts tagged with chemist">chemist</a> might apply Le Chatelier&#8217;s Principle to maximize yield from a reaction.</p>
	Tags: <a href="http://www.kimyaturk.org/tag/chemical-equilibrium/" title="chemical equilibrium" rel="tag">chemical equilibrium</a>, <a href="http://www.kimyaturk.org/tag/chemical-reaction/" title="chemical reaction" rel="tag">chemical reaction</a>, <a href="http://www.kimyaturk.org/tag/chemist/" title="chemist" rel="tag">chemist</a>, <a href="http://www.kimyaturk.org/tag/chemists/" title="chemists" rel="tag">chemists</a>, <a href="http://www.kimyaturk.org/tag/concentration/" title="concentration" rel="tag">concentration</a>, <a href="http://www.kimyaturk.org/tag/disciplines/" title="disciplines" rel="tag">disciplines</a>, <a href="http://www.kimyaturk.org/tag/economic-equilibrium/" title="economic equilibrium" rel="tag">economic equilibrium</a>, <a href="http://www.kimyaturk.org/tag/henry-louis-le-chatelier/" title="henry louis le chatelier" rel="tag">henry louis le chatelier</a>, <a href="http://www.kimyaturk.org/tag/homeostasis/" title="homeostasis" rel="tag">homeostasis</a>, <a href="http://www.kimyaturk.org/tag/karl-ferdinand-braun/" title="karl ferdinand braun" rel="tag">karl ferdinand braun</a>, <a href="http://www.kimyaturk.org/tag/lenz/" title="lenz" rel="tag">lenz</a>, <a href="http://www.kimyaturk.org/tag/partial-pressure/" title="partial pressure" rel="tag">partial pressure</a>, <a href="http://www.kimyaturk.org/tag/principle/" title="principle" rel="tag">principle</a><br />
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		<item>
		<title>Fischer Esterification: 2-ethylhexyl benzoate</title>
		<link>http://www.kimyaturk.org/fischer-esterification-2-ethylhexyl-benzoate/</link>
		<comments>http://www.kimyaturk.org/fischer-esterification-2-ethylhexyl-benzoate/#comments</comments>
		<pubDate>Thu, 02 Sep 2010 01:26:00 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Organic Chemistry]]></category>
		<category><![CDATA[benzoate]]></category>
		<category><![CDATA[catalyst]]></category>
		<category><![CDATA[concentration]]></category>
		<category><![CDATA[dehydration]]></category>
		<category><![CDATA[efficiency]]></category>
		<category><![CDATA[equilibrium]]></category>
		<category><![CDATA[fischer esterification]]></category>
		<category><![CDATA[ill effects]]></category>
		<category><![CDATA[matter of minutes]]></category>
		<category><![CDATA[microwave heating]]></category>
		<category><![CDATA[ptsa]]></category>
		<category><![CDATA[toluene]]></category>

		<guid isPermaLink="false">http://www.kimyaturk.org/fischer-esterification-2-ethylhexyl-benzoate/</guid>
		<description><![CDATA[Fischer esterification can be a time-consuming process, requiring days for a reaction to reach equilibrium. In this article, researchers developed a way to hasten this process by using a specially designed microwave to heat the reaction quickly and evenly and at an increased pressure. In order to test the efficiency of the device, they synthesized [...]]]></description>
			<content:encoded><![CDATA[<p> </p>
<p class="MsoNormal"><a href="http://www.kimyaturk.org/tag/fischer-esterification/" class="st_tag internal_tag" rel="tag" title="Posts tagged with fischer esterification">Fischer esterification</a> can be a time-consuming process, requiring days for a reaction to reach <a href="http://www.kimyaturk.org/tag/equilibrium/" class="st_tag internal_tag" rel="tag" title="Posts tagged with equilibrium">equilibrium</a>. In this article, researchers developed a way to hasten this process by using a specially designed microwave to heat the reaction quickly and evenly and at an increased pressure. In order to test the <a href="http://www.kimyaturk.org/tag/efficiency/" class="st_tag internal_tag" rel="tag" title="Posts tagged with efficiency">efficiency</a> of the device, they synthesized 2-ethylhexyl <a href="http://www.kimyaturk.org/tag/benzoate/" class="st_tag internal_tag" rel="tag" title="Posts tagged with benzoate">benzoate</a> from benzoic acid and 2-ethylhexanol as shown below.</p>
<p class="MsoNormal"><a href="http://photos1.blogger.com/blogger/5493/2291/1600/esterification.1.gif"><img style="margin: 0px auto 10px; display: block; text-align: center; cursor: pointer;" src="http://photos1.blogger.com/blogger/5493/2291/400/esterification.jpg" border="0" alt="" /></a></p>
<p class="MsoNormal">
<p class="MsoNormal">Sulfuric acid as well as para-<a href="http://www.kimyaturk.org/tag/toluene/" class="st_tag internal_tag" rel="tag" title="Posts tagged with toluene">toluene</a> sulfonic acid (<a href="http://www.kimyaturk.org/tag/ptsa/" class="st_tag internal_tag" rel="tag" title="Posts tagged with ptsa">PTSA</a>) were used to catalyze the reaction. In order to shift the reaction towards the products, a large excess of 2-ethylhexanol was used and the water produced was constantly removed. One of the disadvantages of Fischer esterification is that <a href="http://www.kimyaturk.org/tag/dehydration/" class="st_tag internal_tag" rel="tag" title="Posts tagged with dehydration">dehydration</a> can also occur, resulting in unwanted ether and alkene products. Because of this, the temperature and <a href="http://www.kimyaturk.org/tag/catalyst/" class="st_tag internal_tag" rel="tag" title="Posts tagged with catalyst">catalyst</a> <a href="http://www.kimyaturk.org/tag/concentration/" class="st_tag internal_tag" rel="tag" title="Posts tagged with concentration">concentration</a> must be carefully monitored. The researchers were able to show that <a href="http://www.kimyaturk.org/tag/microwave-heating/" class="st_tag internal_tag" rel="tag" title="Posts tagged with microwave heating">microwave heating</a> causes no <a href="http://www.kimyaturk.org/tag/ill-effects/" class="st_tag internal_tag" rel="tag" title="Posts tagged with ill effects">ill effects</a> on the reaction and reduces the time required to a matter of minutes while still producing a high level of the desired product.</p>
<p><a href="http://www.citeulike.org/user/xrockgeekx/article/506551"></a></p>
<div class="blogger-post-footer"><img src="https://blogger.googleusercontent.com/tracker/10660419-114009652016518349?l=chem242.blogspot.com" alt="" width="1" height="1" /></div>
	Tags: <a href="http://www.kimyaturk.org/tag/benzoate/" title="benzoate" rel="tag">benzoate</a>, <a href="http://www.kimyaturk.org/tag/catalyst/" title="catalyst" rel="tag">catalyst</a>, <a href="http://www.kimyaturk.org/tag/concentration/" title="concentration" rel="tag">concentration</a>, <a href="http://www.kimyaturk.org/tag/dehydration/" title="dehydration" rel="tag">dehydration</a>, <a href="http://www.kimyaturk.org/tag/efficiency/" title="efficiency" rel="tag">efficiency</a>, <a href="http://www.kimyaturk.org/tag/equilibrium/" title="equilibrium" rel="tag">equilibrium</a>, <a href="http://www.kimyaturk.org/tag/fischer-esterification/" title="fischer esterification" rel="tag">fischer esterification</a>, <a href="http://www.kimyaturk.org/tag/ill-effects/" title="ill effects" rel="tag">ill effects</a>, <a href="http://www.kimyaturk.org/tag/matter-of-minutes/" title="matter of minutes" rel="tag">matter of minutes</a>, <a href="http://www.kimyaturk.org/tag/microwave-heating/" title="microwave heating" rel="tag">microwave heating</a>, <a href="http://www.kimyaturk.org/tag/ptsa/" title="ptsa" rel="tag">ptsa</a>, <a href="http://www.kimyaturk.org/tag/toluene/" title="toluene" rel="tag">toluene</a><br />
]]></content:encoded>
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		</item>
		<item>
		<title>Chemistry of a Breathalyzer</title>
		<link>http://www.kimyaturk.org/chemistry-of-a-breathalyzer/</link>
		<comments>http://www.kimyaturk.org/chemistry-of-a-breathalyzer/#comments</comments>
		<pubDate>Tue, 31 Aug 2010 09:26:00 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Organic Chemistry]]></category>
		<category><![CDATA[absorbance]]></category>
		<category><![CDATA[alcohol present]]></category>
		<category><![CDATA[alcohols]]></category>
		<category><![CDATA[blood alcohol level]]></category>
		<category><![CDATA[breathalyzer]]></category>
		<category><![CDATA[carboxylic acids]]></category>
		<category><![CDATA[catalyst]]></category>
		<category><![CDATA[chromate ion]]></category>
		<category><![CDATA[color intensity]]></category>
		<category><![CDATA[concentration]]></category>
		<category><![CDATA[ethanol]]></category>
		<category><![CDATA[level chemistry]]></category>
		<category><![CDATA[micrograms]]></category>
		<category><![CDATA[oxidize]]></category>
		<category><![CDATA[oxidizing agent]]></category>
		<category><![CDATA[potassium dichromate]]></category>
		<category><![CDATA[silver nitrate]]></category>
		<category><![CDATA[spectrophotometer]]></category>
		<category><![CDATA[stoichiometric coefficients]]></category>

		<guid isPermaLink="false">http://www.kimyaturk.org/chemistry-of-a-breathalyzer/</guid>
		<description><![CDATA[A Breathalyzer makes use of the fact that alcohols (in this case ethanol) oxidize into carboxylic acids. It uses the strong oxidizing agent Potassium dichromate in a yellow solution of sulfuric acid, under the presence of a Silver Nitrate catalyst, to complete the reaction quickly. As ethanol oxidizes and the Potassium dichromate reacts, the chromate [...]]]></description>
			<content:encoded><![CDATA[<p> A Breathalyzer makes use of the fact that <a href="http://www.kimyaturk.org/tag/alcohols/" class="st_tag internal_tag" rel="tag" title="Posts tagged with alcohols">alcohols</a> (in this case ethanol) <a href="http://www.kimyaturk.org/tag/oxidize/" class="st_tag internal_tag" rel="tag" title="Posts tagged with oxidize">oxidize</a> into carboxylic acids. It uses the strong oxidizing agent <a href="http://www.kimyaturk.org/tag/potassium-dichromate/" class="st_tag internal_tag" rel="tag" title="Posts tagged with potassium dichromate">Potassium dichromate</a> in a yellow solution of sulfuric acid, under the presence of a <a href="http://www.kimyaturk.org/tag/silver-nitrate/" class="st_tag internal_tag" rel="tag" title="Posts tagged with silver nitrate">Silver Nitrate</a> catalyst, to complete the reaction quickly. As ethanol oxidizes and the Potassium dichromate reacts, the chromate ion changes from Cr (VI) to Cr (III). This causes the <a href="http://www.kimyaturk.org/tag/color-intensity/" class="st_tag internal_tag" rel="tag" title="Posts tagged with color intensity">color intensity</a> of the yellow solution to decrease, and a <a href="http://www.kimyaturk.org/tag/spectrophotometer/" class="st_tag internal_tag" rel="tag" title="Posts tagged with spectrophotometer">spectrophotometer</a> in the breathalyzer compares the <a href="http://www.kimyaturk.org/tag/absorbance/" class="st_tag internal_tag" rel="tag" title="Posts tagged with absorbance">absorbance</a> of this solution with that of an unreacted solution</p>
<p><img style="display: block; margin: 0px auto 10px; cursor: hand; text-align: center;" src="http://photos1.blogger.com/blogger/2134/1093/400/breathalyzer1.jpg" border="0" alt="" /></p>
<p>Using Beer&#8217;s law, the spectrophotometer can relate concentration to absorbance levels of the chromium ion. The amount of <a href="http://www.kimyaturk.org/tag/alcohol-present/" class="st_tag internal_tag" rel="tag" title="Posts tagged with alcohol present">alcohol present</a> is proportional to the <a href="http://www.kimyaturk.org/tag/stoichiometric-coefficients/" class="st_tag internal_tag" rel="tag" title="Posts tagged with stoichiometric coefficients">stoichiometric coefficients</a>. An actual breathalyzer only needs to detect 25 <a href="http://www.kimyaturk.org/tag/micrograms/" class="st_tag internal_tag" rel="tag" title="Posts tagged with micrograms">micrograms</a> of ethanol to give a reading 0.10 <a href="http://www.kimyaturk.org/tag/blood-alcohol-level/" class="st_tag internal_tag" rel="tag" title="Posts tagged with blood alcohol level">Blood Alcohol Level</a>.</p>
<p><a href="http://www.citeulike.org/user/ErikofGermany/article/275694"></a></p>
<div class="blogger-post-footer"><img src="https://blogger.googleusercontent.com/tracker/10660419-112330057537530386?l=chem242.blogspot.com" alt="" width="1" height="1" /></div>
	Tags: <a href="http://www.kimyaturk.org/tag/absorbance/" title="absorbance" rel="tag">absorbance</a>, <a href="http://www.kimyaturk.org/tag/alcohol-present/" title="alcohol present" rel="tag">alcohol present</a>, <a href="http://www.kimyaturk.org/tag/alcohols/" title="alcohols" rel="tag">alcohols</a>, <a href="http://www.kimyaturk.org/tag/blood-alcohol-level/" title="blood alcohol level" rel="tag">blood alcohol level</a>, <a href="http://www.kimyaturk.org/tag/breathalyzer/" title="breathalyzer" rel="tag">breathalyzer</a>, <a href="http://www.kimyaturk.org/tag/carboxylic-acids/" title="carboxylic acids" rel="tag">carboxylic acids</a>, <a href="http://www.kimyaturk.org/tag/catalyst/" title="catalyst" rel="tag">catalyst</a>, <a href="http://www.kimyaturk.org/tag/chromate-ion/" title="chromate ion" rel="tag">chromate ion</a>, <a href="http://www.kimyaturk.org/tag/color-intensity/" title="color intensity" rel="tag">color intensity</a>, <a href="http://www.kimyaturk.org/tag/concentration/" title="concentration" rel="tag">concentration</a>, <a href="http://www.kimyaturk.org/tag/ethanol/" title="ethanol" rel="tag">ethanol</a>, <a href="http://www.kimyaturk.org/tag/level-chemistry/" title="level chemistry" rel="tag">level chemistry</a>, <a href="http://www.kimyaturk.org/tag/micrograms/" title="micrograms" rel="tag">micrograms</a>, <a href="http://www.kimyaturk.org/tag/oxidize/" title="oxidize" rel="tag">oxidize</a>, <a href="http://www.kimyaturk.org/tag/oxidizing-agent/" title="oxidizing agent" rel="tag">oxidizing agent</a>, <a href="http://www.kimyaturk.org/tag/potassium-dichromate/" title="potassium dichromate" rel="tag">potassium dichromate</a>, <a href="http://www.kimyaturk.org/tag/silver-nitrate/" title="silver nitrate" rel="tag">silver nitrate</a>, <a href="http://www.kimyaturk.org/tag/spectrophotometer/" title="spectrophotometer" rel="tag">spectrophotometer</a>, <a href="http://www.kimyaturk.org/tag/stoichiometric-coefficients/" title="stoichiometric coefficients" rel="tag">stoichiometric coefficients</a><br />
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