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	<title>Comments for Organic Chemistry Help!</title>
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	<link>http://www.ochemhelp.com</link>
	<description>Homework help, articles, and practice tests for everyone&#039;s favorite subject.</description>
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		<title>Comment on Naming: Ketones by Organic Chemistry Fundamentals: What is a Locant? &#124; Organic Chemistry Help!</title>
		<link>http://www.ochemhelp.com/2011/11/03/naming-ketones/#comment-178</link>
		<dc:creator>Organic Chemistry Fundamentals: What is a Locant? &#124; Organic Chemistry Help!</dc:creator>
		<pubDate>Sun, 18 Dec 2011 02:43:06 +0000</pubDate>
		<guid isPermaLink="false">http://www.ochemhelp.com/?p=88#comment-178</guid>
		<description>[...] say we have a 5-carbon molecule with a ketone functional group. According to ketone nomenclature, the name will be pentanone. Pentan- for the 5 carbon chain, and -one for the ketone primary [...]</description>
		<content:encoded><![CDATA[<p>[...] say we have a 5-carbon molecule with a ketone functional group. According to ketone nomenclature, the name will be pentanone. Pentan- for the 5 carbon chain, and -one for the ketone primary [...]</p>
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	<item>
		<title>Comment on Fundamentals: What is a Locant? by Naming Alkenes: IUPAC, Common Names, and Stereochemistry &#124; Organic Chemistry Help!</title>
		<link>http://www.ochemhelp.com/2011/11/27/fundamentals-what-is-a-locant/#comment-91</link>
		<dc:creator>Naming Alkenes: IUPAC, Common Names, and Stereochemistry &#124; Organic Chemistry Help!</dc:creator>
		<pubDate>Sun, 27 Nov 2011 23:52:19 +0000</pubDate>
		<guid isPermaLink="false">http://www.ochemhelp.com/?p=270#comment-91</guid>
		<description>[...] location of alkyne triple bond with numerical locant, choosing the lower of the two carbons. In this case, the triple bond spans C2-C3, so the locant 2 [...]</description>
		<content:encoded><![CDATA[<p>[...] location of alkyne triple bond with numerical locant, choosing the lower of the two carbons. In this case, the triple bond spans C2-C3, so the locant 2 [...]</p>
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	<item>
		<title>Comment on Fundamentals: What is a Locant? by Naming Ketones: IUPAC and Replacement Nomenclature &#124; Organic Chemistry Help!</title>
		<link>http://www.ochemhelp.com/2011/11/27/fundamentals-what-is-a-locant/#comment-90</link>
		<dc:creator>Naming Ketones: IUPAC and Replacement Nomenclature &#124; Organic Chemistry Help!</dc:creator>
		<pubDate>Sun, 27 Nov 2011 23:51:14 +0000</pubDate>
		<guid isPermaLink="false">http://www.ochemhelp.com/?p=270#comment-90</guid>
		<description>[...] including the carbonyl carbon from the ketone. Then signify the ketone substituent with appropriate locant and -oxo-.    [...]</description>
		<content:encoded><![CDATA[<p>[...] including the carbonyl carbon from the ketone. Then signify the ketone substituent with appropriate locant and -oxo-.    [...]</p>
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	<item>
		<title>Comment on Fundamentals: What is a Locant? by Naming Aromatic Compounds: IUPAC and Common Nomenclature &#124; Organic Chemistry Help!</title>
		<link>http://www.ochemhelp.com/2011/11/27/fundamentals-what-is-a-locant/#comment-89</link>
		<dc:creator>Naming Aromatic Compounds: IUPAC and Common Nomenclature &#124; Organic Chemistry Help!</dc:creator>
		<pubDate>Sun, 27 Nov 2011 23:50:11 +0000</pubDate>
		<guid isPermaLink="false">http://www.ochemhelp.com/?p=270#comment-89</guid>
		<description>[...] locating substituents on a benzene ring, you may either use numeric locants, or the prefixes &#8220;ortho&#8220;, &#8220;meta&#8220;, and &#8220;para&#8220;. These can also be [...]</description>
		<content:encoded><![CDATA[<p>[...] locating substituents on a benzene ring, you may either use numeric locants, or the prefixes &#8220;ortho&#8220;, &#8220;meta&#8220;, and &#8220;para&#8220;. These can also be [...]</p>
]]></content:encoded>
	</item>
	<item>
		<title>Comment on Naming: Amides by Organich Chemistry Fundamentals: What is a Locant? &#124; Organic Chemistry Help!</title>
		<link>http://www.ochemhelp.com/2011/11/11/naming-amides/#comment-88</link>
		<dc:creator>Organich Chemistry Fundamentals: What is a Locant? &#124; Organic Chemistry Help!</dc:creator>
		<pubDate>Sun, 27 Nov 2011 23:48:06 +0000</pubDate>
		<guid isPermaLink="false">http://www.ochemhelp.com/?p=107#comment-88</guid>
		<description>[...] all locants are numbers! When naming amides, the locant &#8220;N&#8221; is often used.   This entry was posted in Fundamentals and tagged [...]</description>
		<content:encoded><![CDATA[<p>[...] all locants are numbers! When naming amides, the locant &#8220;N&#8221; is often used.   This entry was posted in Fundamentals and tagged [...]</p>
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	<item>
		<title>Comment on Fundamentals: Degree of Unsaturation by Practice Problem: Draw 6 Constitutional Isomers for the Molecular Formula C3H8O2 &#124; Organic Chemistry Help!</title>
		<link>http://www.ochemhelp.com/2011/11/26/fundamentals-degree-of-unsaturation/#comment-81</link>
		<dc:creator>Practice Problem: Draw 6 Constitutional Isomers for the Molecular Formula C3H8O2 &#124; Organic Chemistry Help!</dc:creator>
		<pubDate>Sun, 27 Nov 2011 02:26:09 +0000</pubDate>
		<guid isPermaLink="false">http://www.ochemhelp.com/?p=246#comment-81</guid>
		<description>[...] to the degree of unsaturation formula, C3H8O2 has no double bonds or [...]</description>
		<content:encoded><![CDATA[<p>[...] to the degree of unsaturation formula, C3H8O2 has no double bonds or [...]</p>
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		<title>Comment on Fundamentals: Degree of Unsaturation by Practice Problem: Draw 4 non-cyclic constitutional isomers for the molecular formula C4H8 &#124; Organic Chemistry Help!</title>
		<link>http://www.ochemhelp.com/2011/11/26/fundamentals-degree-of-unsaturation/#comment-80</link>
		<dc:creator>Practice Problem: Draw 4 non-cyclic constitutional isomers for the molecular formula C4H8 &#124; Organic Chemistry Help!</dc:creator>
		<pubDate>Sun, 27 Nov 2011 01:55:08 +0000</pubDate>
		<guid isPermaLink="false">http://www.ochemhelp.com/?p=246#comment-80</guid>
		<description>[...] IR Spec       &#8592; Fundamentals: Degree of Unsaturation [...]</description>
		<content:encoded><![CDATA[<p>[...] IR Spec       &larr; Fundamentals: Degree of Unsaturation [...]</p>
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	<item>
		<title>Comment on What is a Halide? by Organic Chemistry Fundamentals: Degrees of Unsaturation &#124; Organic Chemistry Help!</title>
		<link>http://www.ochemhelp.com/2011/11/22/what-is-a-halide/#comment-79</link>
		<dc:creator>Organic Chemistry Fundamentals: Degrees of Unsaturation &#124; Organic Chemistry Help!</dc:creator>
		<pubDate>Sun, 27 Nov 2011 01:39:30 +0000</pubDate>
		<guid isPermaLink="false">http://www.ochemhelp.com/?p=216#comment-79</guid>
		<description>[...] X = # of halogens [...]</description>
		<content:encoded><![CDATA[<p>[...] X = # of halogens [...]</p>
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		<title>Comment on Infrared Spectroscopy (IR) for Beginners by Craig</title>
		<link>http://www.ochemhelp.com/2011/10/22/infrared-spectroscopy-ir-for-beginners/#comment-78</link>
		<dc:creator>Craig</dc:creator>
		<pubDate>Sat, 26 Nov 2011 22:54:45 +0000</pubDate>
		<guid isPermaLink="false">http://www.ochemhelp.com/?p=31#comment-78</guid>
		<description>I have forward your web site to a colleague I hope she finds this as usefull and clear as I have.</description>
		<content:encoded><![CDATA[<p>I have forward your web site to a colleague I hope she finds this as usefull and clear as I have.</p>
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		<title>Comment on Strong Nucleophiles by Nucleophilic Substitution or Elimination? &#124; Organic Chemistry Help!</title>
		<link>http://www.ochemhelp.com/2011/11/19/strong-nucleophiles/#comment-58</link>
		<dc:creator>Nucleophilic Substitution or Elimination? &#124; Organic Chemistry Help!</dc:creator>
		<pubDate>Wed, 23 Nov 2011 20:55:49 +0000</pubDate>
		<guid isPermaLink="false">http://www.ochemhelp.com/?p=172#comment-58</guid>
		<description>[...] there is a strong nucleophile, SN2 is [...]</description>
		<content:encoded><![CDATA[<p>[...] there is a strong nucleophile, SN2 is [...]</p>
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