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  2. Orbital hybridisation - Wikipedia

    en.wikipedia.org/wiki/Orbital_hybridisation

    For this molecule, carbon sp 2 hybridises, because one π (pi) bond is required for the double bond between the carbons and only three σ bonds are formed per carbon atom. In sp 2 hybridisation the 2s orbital is mixed with only two of the three available 2p orbitals, usually denoted 2p x and 2p y. The third 2p orbital (2p z) remains unhybridised.

  3. Periodic table (electron configurations) - Wikipedia

    en.wikipedia.org/wiki/Periodic_table_(electron...

    Og, 118, oganesson : 1s 2 2s 2 2p 6 3s 2 3p 6 4s 2 3d 10 4p 6 5s 2 4d 10 5p 6 6s 2 4f 14 5d 10 6p 6 7s 2 5f 14 6d 10 7p 6 Note that these electron configurations are given for neutral atoms in the gas phase, which are not the same as the electron configurations for the same atoms in chemical environments.

  4. Block (periodic table) - Wikipedia

    en.wikipedia.org/wiki/Block_(periodic_table)

    The p-block, with the p standing for "principal" and azimuthal quantum number 1, is on the right side of the standard periodic table and encompasses elements in groups 13 to 18. Their general electronic configuration is ns 2 np 1–6. Helium, though being the first element in group 18, is not included in the p-block.

  5. Electron configuration - Wikipedia

    en.wikipedia.org/wiki/Electron_configuration

    The superscript 1 for a singly occupied subshell is not compulsory; for example aluminium may be written as either [Ne] 3s 2 3p 1 or [Ne] 3s 2 3p. In atoms where a subshell is unoccupied despite higher subshells being occupied (as is the case in some ions, as well as certain neutral atoms shown to deviate from the Madelung rule ), the empty ...

  6. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    In the case of water, with its 104.5° HOH angle, the OH bonding orbitals are constructed from O(~sp 4.0) orbitals (~20% s, ~80% p), while the lone pairs consist of O(~sp 2.3) orbitals (~30% s, ~70% p). As discussed in the justification above, the lone pairs behave as very electropositive substituents and have excess s character.

  7. Carbon–carbon bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–carbon_bond

    Carbon is one of the few elements that can form long chains of its own atoms, a property called catenation.This coupled with the strength of the carbon–carbon bond gives rise to an enormous number of molecular forms, many of which are important structural elements of life, so carbon compounds have their own field of study: organic chemistry.

  8. Brie Larson on Why the ‘Lessons in Chemistry ... - AOL

    www.aol.com/brie-larson-why-lessons-chemistry...

    SPOILER ALERT: This story contains spoilers from “Introduction to Chemistry,” the series finale of “Lessons in Chemistry,” now streaming on Apple TV+. Elizabeth Zott, hero of the people.

  9. Vinyl group - Wikipedia

    en.wikipedia.org/wiki/Vinyl_group

    In organic chemistry, a vinyl group (abbr. Vi; [1] IUPAC name: ethenyl group [2]) is a functional group with the formula −CH=CH 2. It is the ethylene (IUPAC name: ethene) molecule (H 2 C=CH 2) with one fewer hydrogen atom. The name is also used for any compound containing that group, namely R−CH=CH 2 where R is any other group of atoms.