PreparED Study Materials

CHEM 3010: Organic Chemistry

School: Tennessee State University

Number of Notes and Study Guides Available: 7

Notes

Videos

Molar Mass Calculation: Sr(OH)2 N2O3 NaClO3 Cr2O3 Explained!
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In this chemistry tutorial learn how to calculate the molar mass of various compounds using atomic masses from the periodic table. Discover the molar mass for compounds such as Strontium Hydroxide Dinitrogen Trioxide Sodium Chlorate and Chromium(III) Oxide. A concise guide to understanding molar masses and their real-world applications.

Calculating the Mass Percent Composition of Chloroform (CHCl?)
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In this video, we delve into the concept of percent composition by mass, exemplified through the compound chloroform (CHCl?), which was once employed as an inhalation anesthetic despite its associated toxicity. By calculating the percent composition for each element within the compound, we gain valuable insights into its composition and its potential effects on health and properties.

Crafting Ionic and Net Ionic Equations: Step-by-Step Guide with Exampl
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Discover how to craft balanced, complete ionic, and net ionic equations for various chemical reactions. Learn the significance of aqueous ions and solid state indicators in these equations.

Structures & Classifications of C?H?? Alkyl Groups: From Primary to Te
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Explore the diverse structures of C?H?? alkyl groups and classify them into primary, secondary, or tertiary categories. Through a visualization of carbon atom arrangements, uncover the nuances of n-pentyl, sec-pentyl, tert-pentyl, isopentyl, and neopentyl structures.

Pseudo-Noble Gas Configurations: A Unique Path to Atomic Stability
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Discover the concept of the pseudo-noble gas configuration, differentiating it from the traditional noble gas configuration. Examine examples like tin and indium to illustrate how elements achieve this unique state of stability. Unpack the intriguing intricacies within atomic structures.

Acid Strength Comparison: Isomers and Proton Removal Explained
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This video provides insights into determining the acid strength of various isomers by examining the ease of proton removal and the stability of the resulting anion. By comparing Propanamine to Trimethylamine and Methoxyethane to Propanol, we determine which compounds are more acidic.

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