<?xml version='1.0' encoding='UTF-8'?><?xml-stylesheet href="http://www.blogger.com/styles/atom.css" type="text/css"?><feed xmlns='http://www.w3.org/2005/Atom' xmlns:openSearch='http://a9.com/-/spec/opensearchrss/1.0/' xmlns:georss='http://www.georss.org/georss' xmlns:gd='http://schemas.google.com/g/2005' xmlns:thr='http://purl.org/syndication/thread/1.0'><id>tag:blogger.com,1999:blog-578105257524215131</id><updated>2011-04-22T12:49:10.596+08:00</updated><title type='text'>CJC Chemistry Blog</title><subtitle type='html'>WELCOME...
This a blog about applications of chemistry...!
CONNECT CHEM WITH REAL LIFE EXAMPLES...!</subtitle><link rel='http://schemas.google.com/g/2005#feed' type='application/atom+xml' href='http://cjcchem.blogspot.com/feeds/posts/default'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/578105257524215131/posts/default?max-results=100'/><link rel='alternate' type='text/html' href='http://cjcchem.blogspot.com/'/><link rel='hub' href='http://pubsubhubbub.appspot.com/'/><author><name>1T21 Chem Blog</name><uri>http://www.blogger.com/profile/17556780532560125811</uri><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='http://img2.blogblog.com/img/b16-rounded.gif'/></author><generator version='7.00' uri='http://www.blogger.com'>Blogger</generator><openSearch:totalResults>7</openSearch:totalResults><openSearch:startIndex>1</openSearch:startIndex><openSearch:itemsPerPage>100</openSearch:itemsPerPage><entry><id>tag:blogger.com,1999:blog-578105257524215131.post-7805833445478246836</id><published>2008-07-27T18:32:00.002+08:00</published><updated>2008-07-27T18:37:04.191+08:00</updated><title type='text'>Intro to Organic Chemistry‏</title><content type='html'>Hi,everyone!&lt;br /&gt;&lt;br /&gt;welcome to Intro to Organic Chemistry‏!&lt;br /&gt;Here are some links which may help you understand Organic Chemistry‏ better!&lt;br /&gt;&lt;br /&gt;&lt;a href="http://www.chemguide.co.uk/basicorg/isomermenu.html#top" target="_blank"&gt;www.chemguide.co.uk/basicorg/isomermenu.html#top&lt;/a&gt;Good notes on the topic and examples&lt;br /&gt;&lt;br /&gt;&lt;a href="http://www.creative-chemistry.org.uk/molecules/isomers.htm" target="_blank"&gt;www.creative-chemistry.org.uk/molecules/isomers.htm&lt;/a&gt;Very colourful website; brief summary; good 3D animation&lt;br /&gt;&lt;br /&gt;&lt;a href="http://www.chembio.uoguelph.ca/educmat/chm19104/isomers/" target="_blank"&gt;www.chembio.uoguelph.ca/educmat/chm19104/isomers/&lt;/a&gt;Interesting problems with 3D animations. Click on the links!&lt;br /&gt;&lt;br /&gt;It will only take 20 min of your time if you attempt all the questions.&lt;br /&gt;So, please go and try!!&lt;br /&gt;It will help you...&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/578105257524215131-7805833445478246836?l=cjcchem.blogspot.com' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://cjcchem.blogspot.com/feeds/7805833445478246836/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='http://www.blogger.com/comment.g?blogID=578105257524215131&amp;postID=7805833445478246836' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/578105257524215131/posts/default/7805833445478246836'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/578105257524215131/posts/default/7805833445478246836'/><link rel='alternate' type='text/html' href='http://cjcchem.blogspot.com/2008/07/intro-to-organic-chemistry.html' title='Intro to Organic Chemistry‏'/><author><name>1T21 Chem Blog</name><uri>http://www.blogger.com/profile/17556780532560125811</uri><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='http://img2.blogblog.com/img/b16-rounded.gif'/></author><thr:total>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-578105257524215131.post-1034606024508672201</id><published>2008-05-11T21:49:00.002+08:00</published><updated>2008-12-10T01:02:31.877+08:00</updated><title type='text'></title><content type='html'>&lt;div&gt;&lt;span style="color:#cc0000;"&gt;Thermal conductivity: why do metals conduct heat?&lt;/span&gt;&lt;br /&gt;Everyone knows that touching a metallic surface at room temperature produces a colder sensation than touching a piece of wood or plastic at the same temperature. The very high thermal conductivity of metals allows them to draw heat out of our bodies very efficiently if they are below body temperature. In the same way, a metallic surface that is above body temperature will feel much warmer than one made of some other material. &lt;span style="color:#3333ff;"&gt;The high thermal conductivity of metals is attributed to vibrational excitations of the fluid-like electrons; this excitation spreads through the crystal far more rapidly than it does in non-metallic solids which depend on vibrational motions of atoms which are much heavier and possess greater inertia.&lt;br /&gt;&lt;/span&gt;&lt;a href="http://3.bp.blogspot.com/_cbi1v7qJC1Y/SCdDc5TCaOI/AAAAAAAAABQ/DMl8JlCCaFo/s1600-h/shiny_truck.jpg"&gt;&lt;img id="BLOGGER_PHOTO_ID_5199198458518595810" style="FLOAT: right; MARGIN: 0px 0px 10px 10px; CURSOR: hand" alt="" src="http://3.bp.blogspot.com/_cbi1v7qJC1Y/SCdDc5TCaOI/AAAAAAAAABQ/DMl8JlCCaFo/s320/shiny_truck.jpg" border="0" /&gt;&lt;/a&gt;&lt;br /&gt;&lt;span style="color:#ff0000;"&gt;Appearance: why are metals shiny?&lt;br /&gt;&lt;/span&gt;We usually recognize a metal by its “metallic lustre”, which refers to its ability of reflect light. &lt;span style="color:#3333ff;"&gt;When light falls on a metal, its rapidly changing electromagnetic field induces similar motions in the more loosely-bound electrons near the surface (this could not happen if the electrons were confined to the atomic valence shells.) A vibrating charge is itself an emitter of electromagnetic radiation, so the effect is to cause the metal to re-emit, or reflect, the incident light, producing the shiny appearance.&lt;/span&gt; What color is a metal? With the two exceptions of copper and gold, the closely-spaced levels in the bands allow metals to absorb all wavelengths equally well, so most metals are basically black, but this is ordinarily evident only when the metallic particles are so small that the band structure is not established.&lt;br /&gt;The distinctive color of gold is a consequence of Einstein's theory of special relativity acting on the extremely high momentum of the inner-shell electrons, increasing their mass and causing the orbitals to contract. The outer (5d) electrons are less affected, and this gives rise to increased blue-light absorption, resulting in enhanced reflection of yellow and red light. &lt;/div&gt;&lt;div&gt; &lt;/div&gt;&lt;div&gt;patrick&lt;/div&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/578105257524215131-1034606024508672201?l=cjcchem.blogspot.com' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://cjcchem.blogspot.com/feeds/1034606024508672201/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='http://www.blogger.com/comment.g?blogID=578105257524215131&amp;postID=1034606024508672201' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/578105257524215131/posts/default/1034606024508672201'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/578105257524215131/posts/default/1034606024508672201'/><link rel='alternate' type='text/html' href='http://cjcchem.blogspot.com/2008/05/thermal-conductivity-why-do-metals.html' title=''/><author><name>1T21 Chem Blog</name><uri>http://www.blogger.com/profile/17556780532560125811</uri><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='http://img2.blogblog.com/img/b16-rounded.gif'/></author><media:thumbnail xmlns:media='http://search.yahoo.com/mrss/' url='http://3.bp.blogspot.com/_cbi1v7qJC1Y/SCdDc5TCaOI/AAAAAAAAABQ/DMl8JlCCaFo/s72-c/shiny_truck.jpg' height='72' width='72'/><thr:total>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-578105257524215131.post-7004194712551795952</id><published>2008-05-10T19:41:00.009+08:00</published><updated>2008-12-10T01:02:32.921+08:00</updated><title type='text'></title><content type='html'>&lt;b&gt;&lt;span style=""&gt;A bit on chemical bonding.&lt;/span&gt;&lt;/b&gt;      &lt;p class="MsoNormal"&gt;&lt;b style=""&gt;&lt;u&gt;&lt;span style=""&gt;Hybridisation in methane.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;br /&gt;&lt;span style="line-height: 115%;"&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/u&gt;&lt;/b&gt;&lt;br /&gt;&lt;span style="line-height: 115%;"&gt;This is a common structure of methane that we would normally&lt;/span&gt;&lt;span style="line-height: 115%;"&gt; draw using dot and cross diagram, however, this is a wrong structure.&lt;/span&gt;&lt;/p&gt;&lt;p class="MsoNormal"&gt;&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://3.bp.blogspot.com/_cbi1v7qJC1Y/SCWRLMSPvFI/AAAAAAAAAAo/f5a2dUo6TSw/s1600-h/methane.jpg"&gt;&lt;img style="margin: 0px auto 10px; display: block; text-align: center; cursor: pointer;" src="http://3.bp.blogspot.com/_cbi1v7qJC1Y/SCWRLMSPvFI/AAAAAAAAAAo/f5a2dUo6TSw/s320/methane.jpg" alt="" id="BLOGGER_PHOTO_ID_5198720966331448402" border="0" /&gt;&lt;/a&gt;&lt;/p&gt;&lt;br /&gt;&lt;p class="MsoNormal"&gt;&lt;br /&gt;&lt;/p&gt;&lt;p class="MsoNormal"&gt;  &lt;/p&gt;&lt;p class="MsoNormal"&gt;&lt;span style="line-height: 115%;"&gt;As you all know, the electronic configuration of CH&lt;sub&gt;4­ &lt;/sub&gt;is&lt;/span&gt;&lt;span style="line-height: 115%;"&gt; 1s&lt;sup&gt;2&lt;/sup&gt;2s&lt;sup&gt;2&lt;/sup&gt;2p&lt;sub&gt;x&lt;/sub&gt;&lt;sup&gt;1&lt;/sup&gt;2p&lt;sub&gt;y&lt;/sub&gt;&lt;sup&gt;1&lt;/sup&gt;. This electronic&lt;/span&gt;&lt;span style="line-height: 115%;"&gt; configuration (the 1s&lt;sup&gt;2&lt;/sup&gt; is not shown on the electron in box diagram) shows that only 2 electrons are&lt;/span&gt;&lt;span style="line-height: 115%;"&gt; available for sharing. So why is methane CH&lt;sub&gt;4&lt;/sub&gt; and not CH&lt;sub&gt;2&lt;/sub&gt;?&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoNormal"&gt;&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://1.bp.blogspot.com/_cbi1v7qJC1Y/SCWRbsSPvGI/AAAAAAAAAAw/_zumQ1yuevU/s1600-h/b4hybrid.jpg"&gt;&lt;img style="margin: 0px auto 10px; display: block; text-align: center; cursor: pointer;" src="http://1.bp.blogspot.com/_cbi1v7qJC1Y/SCWRbsSPvGI/AAAAAAAAAAw/_zumQ1yuevU/s320/b4hybrid.jpg" alt="" id="BLOGGER_PHOTO_ID_5198721249799289954" border="0" /&gt;&lt;/a&gt;&lt;/p&gt;&lt;br /&gt;&lt;p class="MsoNormal"&gt;&lt;br /&gt;&lt;/p&gt;&lt;p class="MsoNormal"&gt;  &lt;/p&gt;&lt;p class="MsoNormal" style="line-height: normal;"&gt;&lt;span style=""&gt;When bonds are form, it is an&lt;/span&gt;&lt;span style=""&gt; exothermic reaction and as you all know, energy is released and the whole system is more stable. (Remember your notes? Less&lt;/span&gt;&lt;span style=""&gt; energy = more stable). When&lt;/span&gt;&lt;span style=""&gt; carbon forms 4 bonds (4 C-H bonds), the energy released is twice the energy released when carbon&lt;/span&gt;&lt;span style=""&gt; forming 2 bonds (2 C-H bonds). The energy gap between the 2s&lt;/span&gt;&lt;span style=""&gt; orbital and the 2p orbital is very small and so it pays the carbon to&lt;/span&gt;&lt;span style=""&gt; provide a small amount of energy to promote an electron from the 2s to the empty 2p to give 4 unpaired&lt;/span&gt;&lt;span style=""&gt; electrons. The extra energy released when the bonds form more than compensates for the initial input.&lt;/span&gt;&lt;span style=""&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoNormal"&gt;&lt;span style=""&gt;&lt;o:p&gt; &lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoNormal"&gt;&lt;span style="line-height: 115%;"&gt;If you are unsure and curious about why the arrow is drawn upwards,&lt;/span&gt;&lt;span style="line-height: 115%;"&gt; look down.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoNormal" style="line-height: normal;"&gt;&lt;span style=""&gt;Now that we've got 4 unpaired&lt;/span&gt;&lt;span style=""&gt; electrons ready for bonding, another problem arises. In methane all the carbon-hydrogen bonds are identical, but our electrons are in&lt;/span&gt;&lt;span style=""&gt; two different kinds of orbitals. You aren't going to get four identical&lt;/span&gt;&lt;span style=""&gt; bonds unless you start from four identical orbitals.&lt;/span&gt;&lt;/p&gt;    &lt;p class="MsoNormal" style="line-height: normal;"&gt;  &lt;/p&gt;&lt;p class="MsoNormal" style="line-height: normal;"&gt;&lt;span style=""&gt;Now the fun part&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoNormal" style="line-height: normal;"&gt;&lt;b&gt;&lt;span style=""&gt;Hybridisation&lt;/span&gt;&lt;/b&gt;&lt;span style=""&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoNormal"&gt;  &lt;/p&gt;&lt;p class="MsoNormal" style="line-height: normal;"&gt;&lt;span style=""&gt;The electrons rearrange themselves again in a process called hybridisation. This reorganises the&lt;/span&gt;&lt;span style=""&gt; electrons into four identical hybrid orbitals called sp&lt;sup&gt;3&lt;/sup&gt; hybrids (because they are made from one s orbital&lt;/span&gt;&lt;span style=""&gt; and three p orbitals). You should read "sp3" as "s p three" - not as "s p cubed".&lt;/span&gt;&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://3.bp.blogspot.com/_cbi1v7qJC1Y/SCWR7MSPvHI/AAAAAAAAAA4/1nLRaly8Hh0/s1600-h/sp3.jpg"&gt;&lt;img style="margin: 0px auto 10px; display: block; text-align: center; cursor: pointer;" src="http://3.bp.blogspot.com/_cbi1v7qJC1Y/SCWR7MSPvHI/AAAAAAAAAA4/1nLRaly8Hh0/s320/sp3.jpg" alt="" id="BLOGGER_PHOTO_ID_5198721790965169266" border="0" /&gt;&lt;/a&gt;&lt;/p&gt;&lt;br /&gt;&lt;p class="MsoNormal"&gt;  &lt;/p&gt;&lt;p class="MsoNormal" style="line-height: normal;"&gt;&lt;span style=""&gt;sp&lt;sup&gt;3&lt;/sup&gt; hybrid orbitals look a bit like half a p orbital, and they arrange themselves in space so that they are as far apart as possible. You can picture the nucleus as being at the centre of a tetrahedron (a triangularly based pyramid) with the orbitals pointing to the corners. This explains why methane is tetrahedral in shape.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoNormal" style="margin-bottom: 0.0001pt; line-height: normal;"&gt;&lt;span style=""&gt;  &lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoNormal" style="line-height: normal;"&gt;&lt;span style=""&gt;What happens when the bonds are formed?&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoNormal" style="line-height: normal;"&gt;&lt;span style=""&gt;Remember that hydrogen's electron is in a 1s orbital - a spherically symmetric region of space surrounding the nucleus where there is some fixed chance (say 95%) of finding the electron. When a covalent bond is formed, the atomic orbitals (the orbitals in the individual atoms) merge to produce a new molecular orbital which contains the electron pair which creates the bond.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoNormal"&gt;&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://4.bp.blogspot.com/_cbi1v7qJC1Y/SCWSTcSPvII/AAAAAAAAABA/rR7G-3OIGQA/s1600-h/tetrahedral.jpg"&gt;&lt;img style="margin: 0px auto 10px; display: block; text-align: center; cursor: pointer;" src="http://4.bp.blogspot.com/_cbi1v7qJC1Y/SCWSTcSPvII/AAAAAAAAABA/rR7G-3OIGQA/s320/tetrahedral.jpg" alt="" id="BLOGGER_PHOTO_ID_5198722207576996994" border="0" /&gt;&lt;/a&gt;&lt;/p&gt;&lt;p class="MsoNormal"&gt;  &lt;/p&gt;&lt;p class="MsoNormal" style="text-align: center; line-height: normal;" align="center"&gt;&lt;span style=""&gt;&lt;o:p&gt; &lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoNormal" style="line-height: normal;"&gt;&lt;span style=""&gt;Four molecular orbitals are formed, looking rather like the original sp3 hybrids, but with a hydrogen nucleus embedded in each lobe. Each orbital holds the 2 electrons that we've previously drawn as a dot and a cross.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoNormal" style="line-height: normal;"&gt;&lt;span style=""&gt;The principles involved - promotion of electrons if necessary, then hybridisation, followed by the formation of molecular orbitals - can be applied to any covalently-bound molecule.&lt;/span&gt;&lt;/p&gt;&lt;br /&gt;&lt;p class="MsoNormal" style="line-height: normal;"&gt;&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://3.bp.blogspot.com/_cbi1v7qJC1Y/SCWSiMSPvJI/AAAAAAAAABI/8njN-tOGXWs/s1600-h/ch4.jpg"&gt;&lt;img style="margin: 0px auto 10px; display: block; text-align: center; cursor: pointer;" src="http://3.bp.blogspot.com/_cbi1v7qJC1Y/SCWSiMSPvJI/AAAAAAAAABI/8njN-tOGXWs/s320/ch4.jpg" alt="" id="BLOGGER_PHOTO_ID_5198722460980067474" border="0" /&gt;&lt;/a&gt;&lt;/p&gt;&lt;p class="MsoNormal" style="line-height: normal;"&gt;&lt;br /&gt;&lt;span style=""&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoNormal" style="line-height: normal;"&gt;&lt;span style=""&gt;&lt;o:p&gt; &lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoNormal" style="line-height: normal;"&gt;&lt;span style=""&gt;So why are the arrows drawn all pointing upwards?&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoListParagraphCxSpFirst" style="text-indent: -18pt; line-height: normal;"&gt;&lt;!--[if !supportLists]--&gt;&lt;span style=""&gt;&lt;span style=""&gt;1.&lt;span style=""&gt;      &lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;!--[endif]--&gt;&lt;span style=""&gt;Because the arrow indicates the direction in which the electron spins, either clockwise or anticlockwise and the direction of the magnetic moment it creates when the charged electrons are spinning.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoListParagraphCxSpLast" style="text-indent: -18pt; line-height: normal;"&gt;&lt;!--[if !supportLists]--&gt;&lt;span style=""&gt;&lt;span style=""&gt;2.&lt;span style=""&gt;      &lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;!--[endif]--&gt;&lt;span style=""&gt;If the arrow in 2p­&lt;sub&gt;z&lt;/sub&gt; is pointing downwards, the charged particle will create a magnetic field that attracts another electron, but since the 2s electron has a lower energy level, it will attract the 2p&lt;sub&gt;z&lt;/sub&gt; electron and we will be back to square one.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;  &lt;p class="MsoNormal"&gt;&lt;br /&gt;&lt;/p&gt;&lt;br /&gt;&lt;p class="MsoNormal"&gt;&lt;br /&gt;&lt;/p&gt;&lt;p class="MsoNormal"&gt;Michael&lt;br /&gt;&lt;span style="line-height: 115%;"&gt; &lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/p&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/578105257524215131-7004194712551795952?l=cjcchem.blogspot.com' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://cjcchem.blogspot.com/feeds/7004194712551795952/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='http://www.blogger.com/comment.g?blogID=578105257524215131&amp;postID=7004194712551795952' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/578105257524215131/posts/default/7004194712551795952'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/578105257524215131/posts/default/7004194712551795952'/><link rel='alternate' type='text/html' href='http://cjcchem.blogspot.com/2008/05/bit-on-chemical-bonding.html' title=''/><author><name>1T21 Chem Blog</name><uri>http://www.blogger.com/profile/17556780532560125811</uri><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='http://img2.blogblog.com/img/b16-rounded.gif'/></author><media:thumbnail xmlns:media='http://search.yahoo.com/mrss/' url='http://3.bp.blogspot.com/_cbi1v7qJC1Y/SCWRLMSPvFI/AAAAAAAAAAo/f5a2dUo6TSw/s72-c/methane.jpg' height='72' width='72'/><thr:total>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-578105257524215131.post-8309020816445188996</id><published>2008-05-08T21:19:00.008+08:00</published><updated>2008-12-10T01:02:33.143+08:00</updated><title type='text'>Application of the Ideal Gas Law</title><content type='html'>&lt;a href="http://3.bp.blogspot.com/_cbi1v7qJC1Y/SCMPLbXAsgI/AAAAAAAAAAM/WyxWJayjDTM/s1600-h/tire.gif"&gt;&lt;img id="BLOGGER_PHOTO_ID_5198015083912933890" style="FLOAT: right; MARGIN: 0px 0px 10px 10px; CURSOR: hand" alt="" src="http://3.bp.blogspot.com/_cbi1v7qJC1Y/SCMPLbXAsgI/AAAAAAAAAAM/WyxWJayjDTM/s320/tire.gif" border="0" /&gt;&lt;/a&gt;&lt;br /&gt;&lt;div&gt;&lt;br /&gt;&lt;span style="font-family:verdana;"&gt;Using the &lt;strong&gt;&lt;span style="font-size:180%;color:#ff0000;"&gt;Ideal Gas Law&lt;/span&gt;&lt;/strong&gt;, estimate the reduction of pressure in this tire if there is a change of temperature from &lt;span style="color:#cc66cc;"&gt;20oC&lt;/span&gt;&lt;span style="color:#cc66cc;"&gt; &lt;span style="color:#333333;"&gt;to&lt;/span&gt; -20oC&lt;/span&gt;. Assume the tire to be mounted on a car with an initial pressure of &lt;/span&gt;&lt;span style="font-family:verdana;color:#3366ff;"&gt;32 psi (220640 pa or 4611 psf).&lt;br /&gt;&lt;/span&gt;&lt;a name="Screen1"&gt;&lt;/a&gt;&lt;br /&gt;&lt;span style="font-family:verdana;"&gt;The Ideal Gas Law can be expressed as &lt;strong&gt;&lt;span style="font-size:180%;color:#ff6600;"&gt;PV = NkT&lt;/span&gt;&lt;/strong&gt; where P, V &amp;amp; T are the Pressure, Volume and Temperature, respectively and N is the number of molecules contained within the Volume V and k is a constant.&lt;br /&gt;&lt;/span&gt;&lt;a name="Screen2"&gt;&lt;/a&gt;&lt;br /&gt;&lt;span style="font-family:verdana;"&gt;We have two situations, 1) when the temperature is 20oC and 2) when it is -20oC. For each of these situations the Ideal Gas Law applies and we can write&lt;br /&gt;&lt;/span&gt;&lt;span style="font-size:180%;color:#33cc00;"&gt;&lt;span style="font-family:verdana;"&gt;&lt;strong&gt;P1V1 = NkT1&lt;br /&gt;P2V2 = NkT2&lt;/strong&gt;&lt;br /&gt;&lt;/span&gt;&lt;/span&gt;&lt;a name="Screen3"&gt;&lt;/a&gt;&lt;br /&gt;&lt;span style="font-family:verdana;"&gt;Let's &lt;span style="color:#ffffff;"&gt;&lt;span style="color:#ff6600;"&gt;assume the volume of the tire is not affected by the change of tempe&lt;/span&gt;&lt;/span&gt;&lt;span style="color:#ff9900;"&gt;rature&lt;/span&gt;. Since V1 = V2, then it follows that&lt;br /&gt;&lt;/span&gt;&lt;strong&gt;&lt;span style="font-size:180%;"&gt;&lt;span style="font-family:verdana;"&gt;&lt;span style="color:#ff0000;"&gt;NkT1/P1 = NkT2/P2&lt;/span&gt;&lt;br /&gt;&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;/div&gt;&lt;br /&gt;&lt;div&gt;&lt;span style="font-family:verdana;"&gt;and after canceling &lt;span style="color:#ff6666;"&gt;Nk&lt;/span&gt; from both sides，then we have&lt;br /&gt;&lt;/span&gt;&lt;/div&gt;&lt;br /&gt;&lt;div&gt;&lt;span style="font-family:verdana;"&gt;&lt;span style="font-size:180%;color:#33ccff;"&gt;&lt;strong&gt;T1/P1 = T2/P2&lt;br /&gt;&lt;/strong&gt;&lt;/span&gt;Or&lt;br /&gt;&lt;span style="color:#33ccff;"&gt;&lt;strong&gt;&lt;span style="font-size:180%;"&gt;P2 = P1T2/T1&lt;/span&gt;&lt;/strong&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;&lt;br /&gt;&lt;div&gt;&lt;span style="font-family:verdana;"&gt;&lt;span style="color:#ff6666;"&gt;&lt;strong&gt;(&lt;/strong&gt;&lt;/span&gt;&lt;span style="color:#ff6666;"&gt;&lt;strong&gt;It is also the Gay Lussac's Law)&lt;/strong&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;&lt;br /&gt;&lt;div&gt;&lt;span style="font-family:verdana;"&gt;&lt;/span&gt;&lt;/div&gt;&lt;br /&gt;&lt;div&gt;&lt;span style="font-family:verdana;"&gt;Since we know both temperatures and the initial pressure we can solve this problem once we make some simple unit conversions.&lt;br /&gt;&lt;/span&gt;&lt;a name="Screen4"&gt;&lt;/a&gt;&lt;br /&gt;&lt;span style="font-family:verdana;"&gt;When using the Ideal Gas Law we &lt;strong&gt;&lt;span style="font-size:180%;color:#993399;"&gt;&lt;em&gt;must convert the temperatures to Kelvin.&lt;/em&gt;&lt;/span&gt;&lt;/strong&gt; Recall that&lt;br /&gt;&lt;/span&gt;&lt;span style="font-family:verdana;"&gt;&lt;em&gt;&lt;span style="font-size:130%;color:#ffff00;"&gt;&lt;strong&gt;&lt;span style="color:#3333ff;"&gt;Tk = Tc + 273&lt;/span&gt;&lt;br /&gt;&lt;/strong&gt;&lt;/span&gt;&lt;/em&gt;then T1 = 20 + 273 = 293 K and T2 = -20 + 273 = 253 K.&lt;br /&gt;Therefore T2/T1=1.16and P2 = 32 (1.16) = 37.1psi (255805pa or 5346psf)&lt;br /&gt;&lt;/span&gt;&lt;a name="Screen5"&gt;&lt;/a&gt;&lt;br /&gt;&lt;span style="font-family:verdana;"&gt;You see that the reduction of pressure is significant. Low tire pressure will result in poor gas-mileage. In the case that &lt;strong&gt;&lt;span style="font-size:130%;"&gt;&lt;em&gt;&lt;span style="color:#009900;"&gt;you are traveling a long distance it is best to check your tire pressure, especially at the beginning of the winter months. The onset of warmer summer days will instead provoke a pressure increase。&lt;/span&gt;&lt;/em&gt;&lt;/span&gt;&lt;/strong&gt;&lt;/span&gt;&lt;/div&gt;&lt;div&gt;&lt;span style="font-family:verdana;"&gt;&lt;/span&gt;&lt;/div&gt;&lt;div&gt;&lt;span style="font-family:verdana;"&gt;&lt;/span&gt;&lt;/div&gt;&lt;div&gt;&lt;span style="font-family:verdana;color:#333333;"&gt;CJC 1T21 Wei Feng&lt;/span&gt;&lt;/div&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/578105257524215131-8309020816445188996?l=cjcchem.blogspot.com' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://cjcchem.blogspot.com/feeds/8309020816445188996/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='http://www.blogger.com/comment.g?blogID=578105257524215131&amp;postID=8309020816445188996' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/578105257524215131/posts/default/8309020816445188996'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/578105257524215131/posts/default/8309020816445188996'/><link rel='alternate' type='text/html' href='http://cjcchem.blogspot.com/2008/05/application-of-ideal-gas-law.html' title='Application of the Ideal Gas Law'/><author><name>1T21 Chem Blog</name><uri>http://www.blogger.com/profile/17556780532560125811</uri><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='http://img2.blogblog.com/img/b16-rounded.gif'/></author><media:thumbnail xmlns:media='http://search.yahoo.com/mrss/' url='http://3.bp.blogspot.com/_cbi1v7qJC1Y/SCMPLbXAsgI/AAAAAAAAAAM/WyxWJayjDTM/s72-c/tire.gif' height='72' width='72'/><thr:total>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-578105257524215131.post-2853191634524423285</id><published>2008-05-03T11:35:00.000+08:00</published><updated>2008-05-03T11:36:37.350+08:00</updated><title type='text'></title><content type='html'>This Chemistry blog is for all and please comment (by clicking on the comment link at the end of every post.)&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/578105257524215131-2853191634524423285?l=cjcchem.blogspot.com' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://cjcchem.blogspot.com/feeds/2853191634524423285/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='http://www.blogger.com/comment.g?blogID=578105257524215131&amp;postID=2853191634524423285' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/578105257524215131/posts/default/2853191634524423285'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/578105257524215131/posts/default/2853191634524423285'/><link rel='alternate' type='text/html' href='http://cjcchem.blogspot.com/2008/05/this-chemistry-blog-is-for-all-and.html' title=''/><author><name>1T21 Chem Blog</name><uri>http://www.blogger.com/profile/17556780532560125811</uri><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='http://img2.blogblog.com/img/b16-rounded.gif'/></author><thr:total>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-578105257524215131.post-2635228397696517620</id><published>2008-05-01T18:37:00.002+08:00</published><updated>2008-05-01T18:37:57.129+08:00</updated><title type='text'></title><content type='html'>testingtestingtestingtestingtestingtestingtestingtestingt&lt;br /&gt;estingtestingtestingtestingtestingtestingtestingtestingtestingtestingtesting&lt;br /&gt;testingtestingtestingtestingtestingtestingtestingtestingtestingtestingtestingte&lt;br /&gt;stingtestingtestingtestingtestingtestingtestingtestingtestingtestingtestingtesti&lt;br /&gt;ngtestingtestingtestingtestingtestingtestingtestingtestingtestingtestingtestingtestingtesting&lt;br /&gt;testing&lt;br /&gt;testing&lt;br /&gt;testing&lt;br /&gt;testing&lt;br /&gt;testing&lt;br /&gt;testing&lt;br /&gt;testing&lt;br /&gt;testing&lt;br /&gt;testing&lt;br /&gt;testing&lt;br /&gt;testing&lt;br /&gt;testing&lt;br /&gt;testing&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/578105257524215131-2635228397696517620?l=cjcchem.blogspot.com' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://cjcchem.blogspot.com/feeds/2635228397696517620/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='http://www.blogger.com/comment.g?blogID=578105257524215131&amp;postID=2635228397696517620' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/578105257524215131/posts/default/2635228397696517620'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/578105257524215131/posts/default/2635228397696517620'/><link rel='alternate' type='text/html' href='http://cjcchem.blogspot.com/2008/05/testingtestingtestingtestingtestingtest.html' title=''/><author><name>1T21 Chem Blog</name><uri>http://www.blogger.com/profile/17556780532560125811</uri><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='http://img2.blogblog.com/img/b16-rounded.gif'/></author><thr:total>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-578105257524215131.post-40167577731046422</id><published>2008-05-01T17:55:00.000+08:00</published><updated>2008-05-01T17:56:03.543+08:00</updated><title type='text'></title><content type='html'>testing&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/578105257524215131-40167577731046422?l=cjcchem.blogspot.com' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://cjcchem.blogspot.com/feeds/40167577731046422/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='http://www.blogger.com/comment.g?blogID=578105257524215131&amp;postID=40167577731046422' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/578105257524215131/posts/default/40167577731046422'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/578105257524215131/posts/default/40167577731046422'/><link rel='alternate' type='text/html' href='http://cjcchem.blogspot.com/2008/05/testing.html' title=''/><author><name>1T21 Chem Blog</name><uri>http://www.blogger.com/profile/17556780532560125811</uri><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='http://img2.blogblog.com/img/b16-rounded.gif'/></author><thr:total>0</thr:total></entry></feed>
