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<rss xmlns:dc="http://purl.org/dc/elements/1.1/" version="2.0"><channel><atom:link rel="hub" href="http://tumblr.superfeedr.com/" xmlns:atom="http://www.w3.org/2005/Atom"/><description>For Chemistry Enthusiasts</description><title>Cool Chemistry</title><generator>Tumblr (3.0; @chemcool)</generator><link>http://chemcool.tumblr.com/</link><item><title>Question on Quantum Numbers</title><description>&lt;p&gt;&lt;p class="MsoNormal"&gt;&lt;span&gt;How many electrons with azimuthal quantum number, l = 3 are present in an atom having atomic number 54?&lt;/span&gt;&lt;/p&gt;&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/34565061674</link><guid>http://chemcool.tumblr.com/post/34565061674</guid><pubDate>Mon, 29 Oct 2012 20:00:21 +0530</pubDate><category>Chemistry</category><category>Physical Chemistry</category><category>Atomic Structure</category><category>Quantum Numbers</category></item><item><title>Question on Atomic Weight</title><description>&lt;p&gt;&lt;p class="MsoNormal"&gt;&lt;span&gt;A mono atomic ion has the same atomic number and same atomic weight as its neutral atom. Is this statement true or false?&lt;/span&gt;&lt;/p&gt;&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/34486044213</link><guid>http://chemcool.tumblr.com/post/34486044213</guid><pubDate>Sun, 28 Oct 2012 20:00:35 +0530</pubDate><category>Chemistry</category><category>Physical Chemistry</category><category>Atomic Weight</category><category>Atomic Number</category></item><item><title>Question on Addition Reaction</title><description>&lt;p&gt;&lt;p class="MsoNormal"&gt;&lt;span&gt;When but-3-en-2-ol reacts with aq. HBr, how many products are formed and what are they?&lt;/span&gt;&lt;/p&gt;&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/34415115607</link><guid>http://chemcool.tumblr.com/post/34415115607</guid><pubDate>Sat, 27 Oct 2012 20:00:34 +0530</pubDate><category>Chemistry</category><category>Organic Chemistry</category><category>Alkenes</category><category>Addition Reaction</category></item><item><title>Question on Nucleophilic Strength</title><description>&lt;p&gt;&lt;p class="MsoNormal"&gt;&lt;span&gt;Among CH&lt;sub&gt;3&lt;/sub&gt;&lt;sup&gt;-&lt;/sup&gt;, NH&lt;sub&gt;2&lt;/sub&gt;&lt;sup&gt;-&lt;/sup&gt;, OH&lt;sup&gt;- &lt;/sup&gt;and F&lt;sup&gt;- &lt;/sup&gt;&lt;/span&gt;which one is the best Nucleophile?&lt;/p&gt;&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/34356528188</link><guid>http://chemcool.tumblr.com/post/34356528188</guid><pubDate>Fri, 26 Oct 2012 20:00:19 +0530</pubDate><category>Chemistry</category><category>Organic Chemistry</category><category>Nucleophilic Strength</category></item><item><title>Question on Photochemical Bromination</title><description>&lt;p&gt;&lt;p class="MsoNormal"&gt;What is the relative amounts of 1-bromopropane and 2-bromopropane obtained from the photochemical bromination of propane, if the relative reactivity of 1°&amp;#160;: 2°&amp;#160;: 3° Hydrogens to photochemical bromination is 1&amp;#160;: 82&amp;#160;: 1600?&lt;/p&gt;&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/34296678018</link><guid>http://chemcool.tumblr.com/post/34296678018</guid><pubDate>Thu, 25 Oct 2012 20:00:44 +0530</pubDate><category>Chemistry</category><category>Organic Chemistry</category><category>Photochemical Bromination</category><category>Alkanes</category></item><item><title>Question on Unsaturation</title><description>&lt;p&gt;&lt;p class="MsoNormal"&gt;The Molecular formula of an organic compound is C&lt;sub&gt;10&lt;/sub&gt;H&lt;sub&gt;16&amp;#160;&lt;/sub&gt;and takes 2 moles of hydrogen per mole of it. How many rings are likely to be present in its structure?&lt;/p&gt;&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/34231181943</link><guid>http://chemcool.tumblr.com/post/34231181943</guid><pubDate>Wed, 24 Oct 2012 20:00:44 +0530</pubDate><category>Chemistry</category><category>Organic Chemistry</category><category>Unsaturation</category><category>Degree of Unsaturation</category></item><item><title>Question on Photochemical Chlorination</title><description>&lt;p&gt;&lt;span&gt;Isopentane, (CH&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;CH.CH&lt;sub&gt;2&lt;/sub&gt;.CH&lt;sub&gt;3&lt;/sub&gt; can form four isomeric monochloro derivatives on photochemical Chlorination. How many of these are optically active?&lt;/span&gt;&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/34165085791</link><guid>http://chemcool.tumblr.com/post/34165085791</guid><pubDate>Tue, 23 Oct 2012 19:35:14 +0530</pubDate><category>Chemistry</category><category>Organic Chemistry</category><category>Alkanes</category><category>Photochemical Chlorination</category></item><item><title>Question on Nitrogen Oxides</title><description>&lt;p&gt;&lt;span&gt;Which oxide of Nitrogen is produced on heating a mixture of ammonium sulphate and sodium nitrate?&lt;/span&gt;&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/34098505688</link><guid>http://chemcool.tumblr.com/post/34098505688</guid><pubDate>Mon, 22 Oct 2012 19:59:27 +0530</pubDate><category>Chemistry</category><category>Inorganic Chemistry</category><category>Nitrogen Oxides</category></item><item><title>Question on Gaseous State</title><description>&lt;p&gt;&lt;p class="MsoNormal"&gt;A gas is heated in such a way that its pressure and volume both becomes double. Then by decreasing temperature, some of the molecules of the air have been taken in container to maintain the doubled volume and pressure. Assuming one-fourth of initial number of moles has been taken in for the purpose, by what fraction the temperature must have been raised finally of initial absolute temperature?&lt;/p&gt;&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/34027790313</link><guid>http://chemcool.tumblr.com/post/34027790313</guid><pubDate>Sun, 21 Oct 2012 19:20:10 +0530</pubDate><category>Chemistry</category><category>Physical Chemistry</category><category>Gaseous State</category></item><item><title>Question on Dehydration</title><description>&lt;p&gt;What does Orthophosphoric Acid give on strong heating?&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/33957995836</link><guid>http://chemcool.tumblr.com/post/33957995836</guid><pubDate>Sat, 20 Oct 2012 20:00:24 +0530</pubDate><category>Chemistry</category><category>Inorganic Chemistry</category><category>Phosphorus</category><category>Heating</category></item><item><title>Question on Nodal Planes</title><description>&lt;p&gt;How many nodal planes are present in a p&lt;sub&gt;x&lt;/sub&gt; orbital?&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/33893676713</link><guid>http://chemcool.tumblr.com/post/33893676713</guid><pubDate>Fri, 19 Oct 2012 19:03:38 +0530</pubDate><category>Chemistry</category><category>Physical Chemistry</category><category>Nodal Plane</category><category>Atomic Structure</category></item><item><title>Question on Gaseous State</title><description>&lt;p&gt;&lt;span&gt;If the Compressibility Factor of a gas is less than unity at STP, will the molar volume of the gas be greater or lesser than 22.4L at STP?&lt;/span&gt;&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/33836183619</link><guid>http://chemcool.tumblr.com/post/33836183619</guid><pubDate>Thu, 18 Oct 2012 19:29:37 +0530</pubDate><category>Chemistry</category><category>Physical Chemistry</category><category>Gaseous State</category></item><item><title>Question on pH</title><description>&lt;p&gt;&lt;p class="MsoNormal"&gt;&lt;span&gt;A weak base BOH reacts with 0.1M HCl. The dissociation constant of BOH is 10&lt;sup&gt;–6&lt;/sup&gt;. When 50 ml of 0.1N BOH reacts with HCl, what will the pH of the solution be at the neutralization point of the reaction?&lt;/span&gt;&lt;/p&gt;&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/33772948440</link><guid>http://chemcool.tumblr.com/post/33772948440</guid><pubDate>Wed, 17 Oct 2012 19:56:04 +0530</pubDate><category>Chemistry</category><category>Physical Chemistry</category><category>Ionic Equilibrium</category><category>pH</category></item><item><title>Question on Chemical Kinetics</title><description>&lt;p&gt;&lt;p class="MsoNormal"&gt;&lt;span&gt;If 10&lt;sup&gt;–5&lt;/sup&gt;% reactant molecules cross over the barrier in transition state at 298K, what is the activation barrier needed to cross the transition state?&lt;/span&gt;&lt;/p&gt;&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/33708257519</link><guid>http://chemcool.tumblr.com/post/33708257519</guid><pubDate>Tue, 16 Oct 2012 20:00:18 +0530</pubDate><category>Chemistry</category><category>Physical Chemistry</category><category>Chemical Kinetics</category><category>Arrhenius Equation</category></item><item><title>Question on Qualitative Analysis</title><description>&lt;p&gt;Can Tollen&amp;#8217;s Reagent be used to distinguish between methanoic and ethanoic acids?&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/33640501136</link><guid>http://chemcool.tumblr.com/post/33640501136</guid><pubDate>Mon, 15 Oct 2012 19:52:43 +0530</pubDate><category>Chemistry</category><category>Organic Chemistry</category><category>FGI</category></item><item><title>Question on Redox Reaction</title><description>&lt;p&gt;&lt;p class="MsoNormal"&gt;&lt;span&gt;1 mole of hydrazine, N&lt;sub&gt;2&lt;/sub&gt;H&lt;sub&gt;4&lt;/sub&gt; reacts with one mole of selenic acid, H&lt;sub&gt;2&lt;/sub&gt;SeO&lt;sub&gt;3&lt;/sub&gt;, the latter is reduced to selenium. What is hydrazine converted into? Is it N&lt;sub&gt;2&lt;/sub&gt; or NH&lt;sub&gt;3&lt;/sub&gt;?&lt;/span&gt;&lt;/p&gt;&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/33566417351</link><guid>http://chemcool.tumblr.com/post/33566417351</guid><pubDate>Sun, 14 Oct 2012 19:19:34 +0530</pubDate><category>Chemistry</category><category>Physical Chemistry</category><category>Redox</category><category>Oxidation States</category></item><item><title>Question on Organic Reaction</title><description>&lt;p&gt;An Organic Compound &lt;strong&gt;A&lt;/strong&gt; of molecular formula C&lt;sub&gt;4&lt;/sub&gt;H&lt;sub&gt;10&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; reacts with excess hydrogen bromide to give ethylene dibromide as the only product. What is the name of &lt;strong&gt;A&lt;/strong&gt;?&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/31922267401</link><guid>http://chemcool.tumblr.com/post/31922267401</guid><pubDate>Thu, 20 Sep 2012 19:49:12 +0530</pubDate><category>Chemistry</category><category>Organic Chemistry</category></item><item><title>Question on Nucleophilic Substitution Reaction</title><description>&lt;p&gt;Iodide ion is a good nucleophile as well as a good leaving group in nucleophilic substitution reactions. Is this statement true or false?&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/31860343329</link><guid>http://chemcool.tumblr.com/post/31860343329</guid><pubDate>Wed, 19 Sep 2012 19:59:48 +0530</pubDate><category>Chemistry</category><category>Organic Chemistry</category><category>Nucleophilic Substitution</category><category>Leaving Group</category><category>Nucleophilic Strength</category></item><item><title>Question on Electrophilic Aromatic Substitution</title><description>&lt;p&gt;The following two methods can be used to convert benzene into ethylbenzene;&lt;/p&gt;
&lt;p&gt;1. Reacting benzene with ethyl benzene and aluminium chloride (Friedel Craft&amp;#8217;s Alkylation)&lt;/p&gt;
&lt;p&gt;2. Reacting benzene with acetyl chloride and aluminium chloride to produce methyl phenyl ketone (Friedel Craft&amp;#8217;s Acylation) followed by Clemmensen&amp;#8217;s Reduction&lt;/p&gt;
&lt;p&gt;Which out of the above two is the best suited method and why?&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/31795871423</link><guid>http://chemcool.tumblr.com/post/31795871423</guid><pubDate>Tue, 18 Sep 2012 19:53:15 +0530</pubDate><category>Chemistry</category><category>Organic Chemistry</category><category>Aromatic Chemistry</category></item><item><title>Question on Ring Opening</title><description>&lt;p&gt;Cyclohexane does not undergo ring opening compared to cyclopropane molecule during reactions. Why?&lt;/p&gt;</description><link>http://chemcool.tumblr.com/post/31729624788</link><guid>http://chemcool.tumblr.com/post/31729624788</guid><pubDate>Mon, 17 Sep 2012 19:53:56 +0530</pubDate><category>Chemistry</category><category>Organic Chemistry</category><category>Cycloalkanes</category></item></channel></rss>
