PreparED Study Materials

CHM 2211: Organic Chemistry 2

School: University of Florida

Number of Notes and Study Guides Available: 33

Notes

Study Guides

Videos

Cyclohexane to Adipic Acid: Nylon's Yield Calculations
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Explore the fascinating conversion of cyclohexane and oxygen into adipic acid, essential in nylon manufacture. This video breaks down the calculation of theoretical yield, actual yield, and the resultant percent yield of the process. From molar masses to intricate equations, get a concise understanding of this industrial reaction.

Molecular Formulas: Lewis Structures for N2, HCN, CO2, C3H6, and More
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Discover Lewis structures for various molecular formulas, including N2, HCN, CO2, C3H6, and more. Explore their chemical bonding and structural arrangements.

Chromium & Oxygen: Limiting Reactants & Chromium(III) Oxide Formation
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Unravel the reaction of chromium and oxygen forming chromium(III) oxide. Examine different scenarios to determine the limiting reactant using stoichiometric ratios. Understand how to predict product amounts through these calculations.

Molecule Count in 0.334 g of C?H?: Ethane Analysis
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This instructional video guides you through the process of determining the number of molecules in a given sample. It illustrates the conversion from grams to moles using the molar mass of the substance and then to molecules using Avogadro's number, providing a practical example with ethane (C?H?) to calculate approximately 6.67 x 10²¹ molecules in a 0.334 g sample.

Challenges in Studying Mitochondrial Respiratory Complexes
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Explore the complex challenges scientists face when attempting to extract respiratory complexes from the inner mitochondrial membrane for an in-depth study of their properties and functions."

Conjugate Bases of Brønsted Acids: Formulas and Descriptions
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This video delves into the fundamental concept of conjugate bases in the context of the Brønsted-Lowry theory of acids and bases, explaining how when acids donate protons, they transform into their respective conjugate bases. This understanding is exemplified through the specific reactions of various compounds, illustrating how each Brønsted acid, upon proton donation, gives rise to its corresponding conjugate base.

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