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            <title>
									Chemistry (200 Marks) - Group - II				            </title>
            <link>https://cssforum.net/group-ii/chemistry-200-marks/</link>
            <description>CSS Forum Discussion Board</description>
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							                    <item>
                        <title>Chemistry (200 Marks)</title>
                        <link>https://cssforum.net/group-ii/chemistry-200-marks/#post-23</link>
                        <pubDate>Mon, 15 Sep 2025 13:02:15 +0000</pubDate>
                        <description><![CDATA[CSS CHEMISTRY SYLLABUS
Total Marks: 200
PAPER–I — 100 MARKS
I. Atomic Structure and Quantum Chemistry


Electromagnetic spectrum


Photoelectric effect


Bohr’s atomic model

...]]></description>
                        <content:encoded><![CDATA[<h1>CSS CHEMISTRY SYLLABUS</h1>
<h2>Total Marks: 200</h2>
<h1>PAPER–I — 100 MARKS</h1>
<h2>I. Atomic Structure and Quantum Chemistry</h2>
<ul>
<li>
<p>Electromagnetic spectrum</p>
</li>
<li>
<p>Photoelectric effect</p>
</li>
<li>
<p>Bohr’s atomic model</p>
</li>
<li>
<p>Wave and particle nature of matter</p>
</li>
<li>
<p>de Broglie’s equation</p>
</li>
<li>
<p>Heisenberg’s uncertainty principle</p>
</li>
<li>
<p>Wave functions and Born interpretation of wave functions</p>
</li>
<li>
<p>Probability density</p>
</li>
<li>
<p>Eigen functions and Eigen values</p>
</li>
<li>
<p>Hamiltonian operator</p>
</li>
<li>
<p>Schrödinger wave equation and its solution for particles in one- and three-dimensional boxes</p>
</li>
</ul>
<h2>II. Electrochemistry</h2>
<ul>
<li>
<p>Ions in solution</p>
</li>
<li>
<p>Measurement of conductance and Kohlrausch’s law</p>
</li>
<li>
<p>Mobility of ions and transport number</p>
</li>
<li>
<p>Conductometric titrations</p>
</li>
<li>
<p>Debye–Hückel theory and activity coefficient</p>
</li>
<li>
<p>Determination of activities</p>
</li>
<li>
<p>Redox reactions</p>
</li>
<li>
<p>Spontaneous reactions</p>
</li>
<li>
<p>Electrochemical cells</p>
</li>
<li>
<p>Standard electrode potentials</p>
</li>
<li>
<p>Liquid junction potential</p>
</li>
<li>
<p>Electrochemical series</p>
</li>
<li>
<p>Nernst’s equation</p>
</li>
<li>
<p>Measurement of pH</p>
</li>
<li>
<p>Electrolytic cells</p>
</li>
<li>
<p>Potentiometry</p>
</li>
<li>
<p>Reference and indicator electrodes</p>
</li>
<li>
<p>Fuel cells</p>
</li>
<li>
<p>Corrosion and its prevention</p>
</li>
</ul>
<h2>III. Thermodynamics</h2>
<ul>
<li>
<p>Equations of state</p>
</li>
<li>
<p>Ideal and real gases</p>
</li>
<li>
<p>Van der Waals equation for real gases</p>
</li>
<li>
<p>Critical phenomena and critical constants</p>
</li>
<li>
<p>Four laws of thermodynamics and their applications</p>
</li>
<li>
<p>Thermochemistry</p>
</li>
<li>
<p>Calorimetry</p>
</li>
<li>
<p>Heat capacities and their dependence on temperature, pressure and volume</p>
</li>
<li>
<p>Reversible and non-reversible processes</p>
</li>
<li>
<p>Spontaneous and non-spontaneous processes</p>
</li>
<li>
<p>Hess’s law</p>
</li>
<li>
<p>Born–Haber cycle</p>
</li>
<li>
<p>Relations of entropy and Gibbs free energy with equilibrium constant</p>
</li>
<li>
<p>Gibbs–Helmholtz equation</p>
</li>
<li>
<p>Fugacity and activity</p>
</li>
</ul>
<h2>IV. Chemical Kinetics</h2>
<ul>
<li>
<p>Rate and molecularity of reactions</p>
</li>
<li>
<p>Factors affecting the rate of a chemical reaction</p>
</li>
<li>
<p>Zero-, first-, second- and third-order reactions with the same initial concentrations</p>
</li>
<li>
<p>Half-lives of reactions</p>
</li>
<li>
<p>Experimental techniques for rate determination</p>
</li>
<li>
<p>Methods for determination of order of reaction:</p>
<ul>
<li>
<p>Integration method</p>
</li>
<li>
<p>Half-life method</p>
</li>
<li>
<p>Initial-rate method</p>
</li>
<li>
<p>Graphical method</p>
</li>
</ul>
</li>
<li>
<p>Collision theory</p>
</li>
<li>
<p>Transition state theory</p>
</li>
<li>
<p>Arrhenius equation</p>
</li>
<li>
<p>Rate equations of complex reactions</p>
</li>
</ul>
<h2>V. Surface Chemistry and Catalysis</h2>
<ul>
<li>
<p>Properties of liquids</p>
</li>
<li>
<p>Physical and chemical properties of surfaces</p>
</li>
<li>
<p>Determination of surface area</p>
</li>
<li>
<p>Adsorption and absorption</p>
</li>
<li>
<p>Physical adsorption and chemisorption</p>
</li>
<li>
<p>Adsorption isotherms</p>
</li>
<li>
<p>Langmuir adsorption isotherm</p>
</li>
<li>
<p>Freundlich isotherm</p>
</li>
<li>
<p>Colloids:</p>
<ul>
<li>
<p>Properties</p>
</li>
<li>
<p>Classification</p>
</li>
<li>
<p>Preparation of colloidal systems</p>
</li>
</ul>
</li>
<li>
<p>Surfactants</p>
</li>
<li>
<p>Phase rule</p>
</li>
<li>
<p>Gibbs phase rule</p>
</li>
<li>
<p>One-component systems</p>
</li>
<li>
<p>Two-component systems and their examples</p>
</li>
<li>
<p>Catalysis:</p>
<ul>
<li>
<p>Homogeneous catalysis</p>
</li>
<li>
<p>Heterogeneous catalysis</p>
</li>
<li>
<p>Acid-base catalysis</p>
</li>
<li>
<p>Enzyme catalysis</p>
</li>
</ul>
</li>
</ul>
<h2>VI. Fundamentals of Chemometrics</h2>
<ul>
<li>
<p>Sampling</p>
</li>
<li>
<p>Significant figures</p>
</li>
<li>
<p>Stoichiometric calculations</p>
</li>
<li>
<p>Measurement errors</p>
</li>
<li>
<p>Analysis of variance (ANOVA)</p>
</li>
<li>
<p>Arithmetic mean</p>
</li>
<li>
<p>Median</p>
</li>
<li>
<p>Mode</p>
</li>
<li>
<p>Standard deviation and relative standard deviation</p>
</li>
<li>
<p>Confidence limits</p>
</li>
<li>
<p>Gaussian distribution</p>
</li>
<li>
<p>Least-square method</p>
</li>
<li>
<p>Statistical tests</p>
</li>
</ul>
<h2>VII. Separation Methods</h2>
<h3>Solvent Extraction</h3>
<ul>
<li>
<p>Theory of solvent extraction</p>
</li>
<li>
<p>Solvent extraction of metals</p>
</li>
<li>
<p>Analytical separations</p>
</li>
<li>
<p>Multiple batch extraction</p>
</li>
<li>
<p>Counter-current distribution</p>
</li>
</ul>
<h3>Chromatography</h3>
<ul>
<li>
<p>Theory of chromatography</p>
</li>
<li>
<p>Classification and overview of chromatographic techniques:</p>
<ul>
<li>
<p>Paper chromatography</p>
</li>
<li>
<p>Thin-layer chromatography</p>
</li>
<li>
<p>Column chromatography</p>
</li>
<li>
<p>Ion-exchange chromatography</p>
</li>
</ul>
</li>
<li>
<p>Principle of electrophoresis</p>
</li>
<li>
<p>Applications of electrophoresis in separation and characterization of proteins</p>
</li>
</ul>
<h2>VIII. Basic Inorganic Chemistry</h2>
<ul>
<li>
<p>Types of chemical bonding</p>
</li>
<li>
<p>Ionic and covalent bonding</p>
</li>
<li>
<p>Localized bond approach</p>
</li>
<li>
<p>Theories of chemical bonding</p>
</li>
<li>
<p>Valence Bond Theory (VBT)</p>
</li>
<li>
<p>Hybridization and resonance</p>
</li>
<li>
<p>Prediction of molecular shapes using the Valence Shell Electron Pair Repulsion (VSEPR) model</p>
</li>
<li>
<p>Molecular Orbital Theory (MOT) applied to diatomic molecules</p>
</li>
<li>
<p>Delocalized approach to bonding</p>
</li>
<li>
<p>Bonding in electron-deficient compounds</p>
</li>
<li>
<p>Hydrogen bonding</p>
</li>
<li>
<p>Physical and chemical properties of p-block elements, with emphasis on:</p>
<ul>
<li>
<p>Oxygen</p>
</li>
<li>
<p>Carbon</p>
</li>
<li>
<p>Chlorine</p>
</li>
<li>
<p>Silicon</p>
</li>
<li>
<p>Nitrogen</p>
</li>
<li>
<p>Phosphorus</p>
</li>
</ul>
</li>
<li>
<p>Representative compounds of the above elements</p>
</li>
</ul>
<h2>IX. Acids and Bases</h2>
<ul>
<li>
<p>Brief concepts of chemical equilibrium</p>
</li>
<li>
<p>Acid-base theories</p>
</li>
<li>
<p>Soft and Hard Acid and Base (SHAB) concept</p>
</li>
<li>
<p>Relative strength of acids and bases</p>
</li>
<li>
<p>Significance of pH, pKa and pKb</p>
</li>
<li>
<p>Buffer solutions</p>
</li>
<li>
<p>Theory of indicators</p>
</li>
<li>
<p>Solubility</p>
</li>
<li>
<p>Solubility product</p>
</li>
<li>
<p>Common-ion effect</p>
</li>
<li>
<p>Industrial applications</p>
</li>
</ul>
<h2>X. Chemistry of d- and f-Block Elements</h2>
<h3>d-Block Elements</h3>
<ul>
<li>
<p>General characteristics of d-block elements</p>
</li>
<li>
<p>Historical background of coordination chemistry</p>
</li>
<li>
<p>Nomenclature and structure of coordination complexes with coordination numbers 2–10</p>
</li>
<li>
<p>Chelates and chelate effect</p>
</li>
<li>
<p>Theories of coordination complexes:</p>
<ul>
<li>
<p>Werner’s theory</p>
</li>
<li>
<p>Valence Bond Theory (VBT)</p>
</li>
<li>
<p>Crystal Field Theory (CFT)</p>
</li>
<li>
<p>Molecular Orbital Theory (MOT)</p>
</li>
</ul>
</li>
<li>
<p>Jahn–Teller theorem</p>
</li>
<li>
<p>Magnetic properties</p>
</li>
<li>
<p>Spectral properties</p>
</li>
<li>
<p>Isomerism</p>
</li>
<li>
<p>Stereochemistry</p>
</li>
<li>
<p>Stability constants of coordination complexes</p>
</li>
</ul>
<h3>f-Block Elements</h3>
<h4>Lanthanides</h4>
<ul>
<li>
<p>General characteristics</p>
</li>
<li>
<p>Occurrence</p>
</li>
<li>
<p>Extraction and general principles of separation</p>
</li>
<li>
<p>Electronic structure and position in the periodic table</p>
</li>
<li>
<p>Lanthanide contraction</p>
</li>
<li>
<p>Oxidation states</p>
</li>
<li>
<p>Spectral and magnetic properties</p>
</li>
<li>
<p>Uses</p>
</li>
</ul>
<h4>Actinides</h4>
<ul>
<li>
<p>General characteristics</p>
</li>
<li>
<p>Electronic structure</p>
</li>
<li>
<p>Oxidation states</p>
</li>
<li>
<p>Position in the periodic table</p>
</li>
<li>
<p>Half-life</p>
</li>
<li>
<p>Decay law</p>
</li>
</ul>
<hr />
<h1>PAPER–II — 100 MARKS</h1>
<h2>I. Basic Concepts of Organic Chemistry</h2>
<ul>
<li>
<p>Bonding and orbital hybridization</p>
</li>
<li>
<p>Localized and delocalized bonding</p>
</li>
<li>
<p>Inductive effect</p>
</li>
<li>
<p>Dipole moment</p>
</li>
<li>
<p>Resonance</p>
</li>
<li>
<p>Hyperconjugation</p>
</li>
</ul>
<h2>II. Saturated and Unsaturated Hydrocarbons</h2>
<ul>
<li>
<p>Nomenclature</p>
</li>
<li>
<p>Physical properties</p>
</li>
<li>
<p>Preparation and reactions of:</p>
<ul>
<li>
<p>Alkanes</p>
</li>
<li>
<p>Alkenes</p>
</li>
<li>
<p>Alkynes</p>
</li>
</ul>
</li>
</ul>
<h2>III. Chemistry of Aromatic Compounds</h2>
<ul>
<li>
<p>Benzene structure</p>
</li>
<li>
<p>Aromaticity</p>
</li>
<li>
<p>Mechanism of electrophilic substitution reactions</p>
</li>
<li>
<p>Activating and deactivating substituents</p>
</li>
<li>
<p>Effect of substituents on orientation and reactivity</p>
</li>
</ul>
<h2>IV. Chemistry of Functional Groups</h2>
<ul>
<li>
<p>Preparation and properties of:</p>
<ul>
<li>
<p>Alcohols</p>
</li>
<li>
<p>Phenols</p>
</li>
<li>
<p>Ethers</p>
</li>
<li>
<p>Amines</p>
</li>
</ul>
</li>
<li>
<p>Reaction mechanisms and applications</p>
</li>
<li>
<p>Preparation and reactions of alkyl halides</p>
</li>
<li>
<p>Synthetic applications of Grignard reagent</p>
</li>
<li>
<p>Carbonyl compounds</p>
</li>
<li>
<p>Preparation and reaction mechanisms of aldehydes and ketones</p>
</li>
<li>
<p>Applications of aldehydes and ketones</p>
</li>
<li>
<p>Carboxylic acids and their derivatives</p>
</li>
<li>
<p>Acidity of carboxylic acids</p>
</li>
<li>
<p>Effect of substituents on acidity</p>
</li>
<li>
<p>Preparation and reactions of carboxylic acids and their derivatives, including:</p>
<ul>
<li>
<p>Acid halides</p>
</li>
<li>
<p>Acid anhydrides</p>
</li>
<li>
<p>Esters</p>
</li>
<li>
<p>Amides</p>
</li>
</ul>
</li>
</ul>
<h2>V. Aliphatic Nucleophilic Substitution and Elimination Reactions</h2>
<ul>
<li>
<p>Mechanism of nucleophilic substitution reactions</p>
</li>
<li>
<p>Elimination reactions</p>
</li>
<li>
<p>Zaitsev rule</p>
</li>
<li>
<p>Hofmann rule</p>
</li>
<li>
<p>Competition between substitution and elimination reactions</p>
</li>
</ul>
<h2>VI. Stereochemistry</h2>
<ul>
<li>
<p>Molecular chirality</p>
</li>
<li>
<p>Types of stereoisomers</p>
</li>
<li>
<p>R/S and E/Z notation</p>
</li>
<li>
<p>Optical activity</p>
</li>
<li>
<p>Stereoselectivity</p>
</li>
<li>
<p>Stereospecificity</p>
</li>
<li>
<p>Resolution of racemic mixtures</p>
</li>
</ul>
<h2>VII. Organic Spectroscopy</h2>
<ul>
<li>
<p>Theory, principles, instrumentation and applications of:</p>
<ul>
<li>
<p>UV/Visible spectroscopy</p>
</li>
<li>
<p>¹H NMR spectroscopy</p>
</li>
<li>
<p>IR spectroscopy</p>
</li>
<li>
<p>Mass spectroscopic techniques</p>
</li>
</ul>
</li>
</ul>
<h2>VIII. Biomolecules</h2>
<h3>Carbohydrates</h3>
<ul>
<li>
<p>Monosaccharides</p>
</li>
<li>
<p>Oligosaccharides</p>
</li>
<li>
<p>Polysaccharides</p>
</li>
<li>
<p>Biological functions of:</p>
<ul>
<li>
<p>Starch</p>
</li>
<li>
<p>Glycogen</p>
</li>
<li>
<p>Cellulose</p>
</li>
<li>
<p>Cell-wall polysaccharides</p>
</li>
</ul>
</li>
</ul>
<h3>Lipids</h3>
<ul>
<li>
<p>Classification of lipids</p>
</li>
<li>
<p>Biological importance of lipids</p>
</li>
<li>
<p>Significance of lipids in biological membranes</p>
</li>
<li>
<p>Transport mechanisms</p>
</li>
</ul>
<h3>Amino Acids</h3>
<ul>
<li>
<p>Chemistry and classification of amino acids</p>
</li>
<li>
<p>Physical and chemical properties</p>
</li>
<li>
<p>Biological significance</p>
</li>
</ul>
<h3>Proteins</h3>
<ul>
<li>
<p>Classification</p>
</li>
<li>
<p>Properties</p>
</li>
<li>
<p>Biological significance</p>
</li>
<li>
<p>Primary structure</p>
</li>
<li>
<p>Secondary structure</p>
</li>
<li>
<p>Tertiary structure</p>
</li>
<li>
<p>Quaternary structure</p>
</li>
</ul>
<h3>Nucleic Acids</h3>
<ul>
<li>
<p>Chemical composition of nucleic acids</p>
</li>
<li>
<p>Structure of nucleic acids</p>
</li>
<li>
<p>Biological significance of nucleic acids</p>
</li>
</ul>
<h3>Enzymes</h3>
<ul>
<li>
<p>Enzyme-substrate interactions</p>
</li>
<li>
<p>Nature of the active site</p>
</li>
<li>
<p>Mechanism of enzyme action</p>
</li>
<li>
<p>Kinetics of single-substrate reactions</p>
</li>
<li>
<p>Enzyme inhibition</p>
</li>
<li>
<p>Regulatory enzymes</p>
</li>
<li>
<p>Allosteric enzymes</p>
</li>
</ul>
<h2>IX. Metabolism</h2>
<h3>Digestion and Absorption</h3>
<ul>
<li>
<p>Digestion, absorption and transport of:</p>
<ul>
<li>
<p>Proteins</p>
</li>
<li>
<p>Carbohydrates</p>
</li>
<li>
<p>Lipids</p>
</li>
<li>
<p>Nucleic acids</p>
</li>
</ul>
</li>
</ul>
<h3>Carbohydrate Metabolism</h3>
<ul>
<li>
<p>Glycolysis</p>
</li>
<li>
<p>Citric acid cycle</p>
</li>
<li>
<p>Gluconeogenesis</p>
</li>
<li>
<p>Glycogenesis</p>
</li>
<li>
<p>Glycogenolysis</p>
</li>
<li>
<p>Photosynthesis</p>
</li>
</ul>
<h3>Lipid and Amino Acid Metabolism</h3>
<ul>
<li>
<p>Biosynthesis of triglycerides, phospholipids, steroids and bile acids</p>
</li>
<li>
<p>Ketone bodies</p>
</li>
<li>
<p>Biochemical reactions of amino acids:</p>
<ul>
<li>
<p>Decarboxylation</p>
</li>
<li>
<p>Deamination</p>
</li>
<li>
<p>Transamination</p>
</li>
<li>
<p>Transmethylation</p>
</li>
</ul>
</li>
<li>
<p>Urea cycle</p>
</li>
<li>
<p>Creatine synthesis</p>
</li>
<li>
<p>Uric acid synthesis</p>
</li>
<li>
<p>Catabolism of nucleosides</p>
</li>
<li>
<p>DNA polymerases and other enzymes involved in metabolism</p>
</li>
</ul>
<h2>X. Chemical Industries</h2>
<ul>
<li>
<p>Manufacturing and processing of:</p>
<ul>
<li>
<p>Sugar</p>
</li>
<li>
<p>Cement</p>
</li>
<li>
<p>Glass</p>
</li>
<li>
<p>Paper</p>
</li>
<li>
<p>Fertilizers</p>
</li>
<li>
<p>Soap</p>
</li>
<li>
<p>Detergents</p>
</li>
</ul>
</li>
</ul>
<hr />
<h1>SUGGESTED READINGS</h1>
<table>
<thead>
<tr>
<th align="right">S. No.</th>
<th>Title</th>
<th>Author</th>
</tr>
</thead>
<tbody>
<tr>
<td align="right">1</td>
<td><em>Physical Chemistry</em>, 4th ed., 2005</td>
<td>Silbey, R. J., Alberty, R. A., and Bawendi, M. G.</td>
</tr>
<tr>
<td align="right">2</td>
<td><em>Physical Chemistry – A Molecular Approach</em>, 1st ed., 1997</td>
<td>McQuarrie, D. A. and Simon, J. D.</td>
</tr>
<tr>
<td align="right">3</td>
<td><em>Atkin’s Physical Chemistry</em>, 9th ed., 2010</td>
<td>Atkins, P. and Paula, J. D.</td>
</tr>
<tr>
<td align="right">4</td>
<td><em>Physical Chemistry</em>, 4th ed., 1972</td>
<td>Moore, W. J.</td>
</tr>
<tr>
<td align="right">5</td>
<td><em>Modern Analytical Chemistry</em>, 2000</td>
<td>Harvey, D.</td>
</tr>
<tr>
<td align="right">6</td>
<td><em>Quantitative Chemical Analysis</em>, 8th ed., 2011</td>
<td>Harris, D. C.</td>
</tr>
<tr>
<td align="right">7</td>
<td><em>Analytical Chemistry</em>, 6th ed., 2006</td>
<td>Christian, G. D.</td>
</tr>
<tr>
<td align="right">8</td>
<td><em>Chemometrics: Statistics and Computer Applications in Analytical Chemistry</em>, 2nd ed., 2007</td>
<td>Matthios, O.</td>
</tr>
<tr>
<td align="right">9</td>
<td><em>Statistics and Chemometrics for Analytical Chemistry</em>, 5th ed., 2005</td>
<td>Miller, J. and Miller, J.</td>
</tr>
<tr>
<td align="right">10</td>
<td><em>Separation Chemistry</em>, 2004</td>
<td>Budhiraja, R. P.</td>
</tr>
<tr>
<td align="right">11</td>
<td><em>Advanced Inorganic Chemistry</em>, 6th ed., 2007</td>
<td>Cotton, F. A. and Wilkinson, G.</td>
</tr>
<tr>
<td align="right">12</td>
<td><em>Inorganic Chemistry</em>, 4th ed., 2010</td>
<td>Miessler, G. L. and Tarr, D. A.</td>
</tr>
<tr>
<td align="right">13</td>
<td><em>Inorganic Chemistry</em>, 5th ed., 2010</td>
<td>Shriver, D. and Atkins, P.</td>
</tr>
<tr>
<td align="right">14</td>
<td><em>Textbook of Inorganic Chemistry</em>, 2013</td>
<td>Chaudhary, S. U.</td>
</tr>
<tr>
<td align="right">15</td>
<td><em>Organic Chemistry</em>, 10th ed., 2011</td>
<td>Solomons, T. W. G. and Fryhle, C. B.</td>
</tr>
<tr>
<td align="right">16</td>
<td><em>Organic Chemistry</em>, 6th ed., 2012</td>
<td>Brown, W. H., Fotte, C. S., Iverson, B. L. and Anslyn, E. V.</td>
</tr>
<tr>
<td align="right">17</td>
<td><em>Organic Chemistry</em>, 8th ed., 2012</td>
<td>John, E. M.</td>
</tr>
<tr>
<td align="right">18</td>
<td><em>Introduction to Spectroscopy</em>, 4th ed., 2009</td>
<td>Pavia, D. L., Lampman, G. M., Kriz, G. S. and Vyvyan, J. R.</td>
</tr>
<tr>
<td align="right">19</td>
<td><em>Spectrometric Identification of Organic Compounds</em>, 2005</td>
<td>Silverstein, R. M., Webster, F. X. and Kiemle, D.</td>
</tr>
<tr>
<td align="right">20</td>
<td><em>Organic Spectroscopy</em>, 2006</td>
<td>Younas, M.</td>
</tr>
<tr>
<td align="right">21</td>
<td><em>Stereochemistry (Basic Concepts in Chemistry)</em>, 2002</td>
<td>Morris, D. G.</td>
</tr>
<tr>
<td align="right">22</td>
<td><em>Shreve’s Chemical Process Industries</em>, 5th ed., 1984</td>
<td>Shreve, R. N. and Austin, G. T.</td>
</tr>
<tr>
<td align="right">23</td>
<td><em>Riegel’s Handbook of Industrial Chemistry</em>, 2003</td>
<td>Riegel, E. R. and Kent, J. A.</td>
</tr>
</tbody>
</table>]]></content:encoded>
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