Type of C-C bond Pi (double) C hybridization sp2 Bond angle 120 Shape Trigonal Planar Rotation C=C atoms cannot rotate Structure Can be linear, branched, or cyclic Figure 3: Alkenes examples It should be noted that not all alkenes are unsaturated hydrocarbons. To rule out the confusion, si...
Benzene is cyclic, all carbons have sp2 hybridization, it’s a planar ring, and it has six pi electrons. Six is a Huckel’s rule number, so that makes it aromatic! Benzene is far from the only aromatic molecule, however; there are tons. Aromatic vs antiaromatic If a molecule satisfies...
UV-Vis Spectroscopy of Conjugated Alkenes 8m Woodward-Fieser Rules 16m 18. Aromaticity2h 34m Aromaticity 8m Huckel's Rule 10m Pi Electrons 7m Aromatic Hydrocarbons 18m Annulene 17m Aromatic Heterocycles 20m Frost Circle 17m Naming Benzene Rings ...
So we just drew the first two metabolites of the citric acid cycle based on the hints that we talked about previously and these memory tools that we have here. So, click on the next video and let's continue our discussion of the structures of the TCA cy...
Step-by-Step SolutionStep 1: Definition of Aromatic Compounds Aromatic compounds are a class of compounds that are characterized by their cyclic structure, planar geometry, and the presence of delocalized pi el
Hybridization Video duration: 3m 10 concept Molecular Polarity Video duration: 2m 11 concept Functional Groups Video duration: 2m Get better grades in your Organic Chemistry course Watch step-by-step video tutorials that guide you through every chapter in your textbook. Learn the toughest concepts wi...
Acid-Base Properties of Nitrogen Heterocycles 10m Reactions of Pyrrole, Furan, and Thiophene 13m Directing Effects in Substituted Pyrroles, Furans, and Thiophenes 16m Addition Reactions of Furan 8m EAS Reactions of Pyridine 17m SNAr Reactions of Pyridine ...