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Chapter 4 Alkanes: Nomenclature, Conformational Analysis, and an Introduction to Synthesis

Chapter 4 Alkanes: Nomenclature, Conformational Analysis, and an Introduction to Synthesis

Chapter 4 Alkanes: Nomenclature, Conformational Analysis, and an Introduction to Synthesis. Shapes of Alkanes “Straight-chain” alkanes have a zig-zag orientation when they are in their most straight orientation Straight chain alkanes are also called unbranched alkanes.

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1.74k views • 146 slides
Planets

Planets

Planets. Comparative Planetology Astronomy Physics Geology Chemistry Meteorology Biology. What is in the Solar System?. The Sun and some stuff “some stuff” = Jupiter and other stuff “other stuff” = Saturn and more stuff “more stuff” = Uranus, Neptune, and who cares?

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713 views • 34 slides
Organic Chemistry

Organic Chemistry

Unit X. Organic Chemistry . Shelly Wei Mathew Jiang Johnny Yu Mike Chi. A prior question:. What is ORGANIC CHEMISTRY ?.

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308 views • 17 slides
Chapter 16.1

Chapter 16.1

Chapter 16.1. Functions of Proteins. SWBAT: Classify proteins by their functions in the cells. Proteins. Proteins are polymers of amino acids chemically bonded to each other All proteins in humans are made up from 20 different amino acids Protein Subclasses are:

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304 views • 14 slides
Synthesis of Aspirin Prodrugs of β-Cyclodextrin on the Primary/Secondary Hydroxyl Sides

Synthesis of Aspirin Prodrugs of β-Cyclodextrin on the Primary/Secondary Hydroxyl Sides

Aspirin was covalently conjugated to the primary/secondary hydroxyl groups of β-cyclodextrin in different solvents using different reagents for acylation. In pyridine, β-cyclodextrin reacted with acetylsalicylic acid chloride to produce the aspirin conjugates on the primary hydroxyl side, and in a carbonate buffer solution of N, N-dimethylformamide, β-cyclodextrin reacted with N-(2-acetoxybenzoyl)imidazole to give the aspirin conjugates on the secondary hydroxyl side.

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46 views • 3 slides

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