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CH 19
CH 19

Definition: the term “alkaloid” (alkali
Definition: the term “alkaloid” (alkali

E Reprint 212 - Trade Science Inc
E Reprint 212 - Trade Science Inc

Photocatalytic reduction of aromatic azides to amines using CdS
Photocatalytic reduction of aromatic azides to amines using CdS

Full-Text PDF
Full-Text PDF

... presence of two ortho positions. The result in entry 7 reinforces the regioselectivity shown in entry 1. A special case of discussion is entry 10 vs. 7. In the first case, where the ortho and para positions were flanked by two substituents, the ortho one was favored. This observation indicates that ...
ALDEHYDES & KETONES - Rogue Community College
ALDEHYDES & KETONES - Rogue Community College

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CHEM 494 Lecture 10b - UIC Department of Chemistry

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... DH0rxn = [ 12x–393.5 + 6x–285.8 ] – [ 2x49.04 ] = -6534.9 kJ - 6534.9 kJ = - 3267.44 kJ/mol C6H6 2 mol ...
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CfE Advanced Higher Chemistry Unit 2: Organic

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Chemistry 1110 – Organic Chemistry IUPAC Nomenclature

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7. Organic halides

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IR handout

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Unsaturated Hydrocarbons
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... (a) Aniline, p-nitroaniline and p-toluidine p-nitroaniline < ...
Ch 19 Aldehydes and Ketones
Ch 19 Aldehydes and Ketones

... - Aldehydes are more reactive than ketones for both steric and electronic reasons. - First, the H creates less steric hindrance so that the carbonyl C is more accessible. - Second, an organic group provides e- donating induction which stabilizes the + carbonyl C and makes it less reactive. - Formal ...
asymmetric alkyne addition to aldehydes
asymmetric alkyne addition to aldehydes

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ENGLISH VERSION Exam Organic Chemistry 2

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Chapter 13 – Organic Chemistry

... Indeed, straight chain hydrocarbons react so fast and violently that they can cause an engine to “knock.” The octane rating of a gasoline indicates the extent of knocking it causes. The reference molecules are shown in Figure 13.4. The straight chain hydrocarbon C7 H16 causes substantial knocking a ...
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Aromatization

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