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Ethanethiol, commonly known as ethyl mercaptan, is an organosulfur compound with the formula CH 3 CH 2 SH. [5] It is a colorless liquid with a distinct odor. Abbreviated EtSH, it consists of an ethyl group (Et), CH 3 CH 2, attached to a thiol group, SH. Its structure parallels that of ethanol, but with sulfur in place of oxygen. The odor of ...
In organic chemistry, a thiol (/ ˈ θ aɪ ɒ l /; [1] from Ancient Greek θεῖον (theion) 'sulfur' [2]), or thiol derivative, is any organosulfur compound of the form R−SH, where R represents an alkyl or other organic substituent. The −SH functional group itself is referred to as either a thiol group or a sulfhydryl group, or a ...
Like 1,3-propanedithiol, 1,2-ethanedithiol readily forms metal thiolate complexes. Illustrative is the synthesis of the derivative diiron ethanedithiolate hexacarbonyl upon reaction with triiron dodecacarbonyl: [5] Fe 3 (CO) 12 + C 2 H 4 (SH) 2 → Fe 2 (S 2 C 2 H 4)(CO) 6 + H 2 + Fe(CO) 5 + CO
Ten years after James Watson and Francis Crick published their model of the DNA double helix, [2] Karst Hoogsteen reported [3] a crystal structure of a complex in which analogues of A and T formed a base pair that had a different geometry from that described by Watson and Crick. Similarly, an alternative base-pairing geometry can occur for G ...
In the gas phase, a single water molecule has an oxygen atom surrounded by two hydrogens and two lone pairs, and the H 2 O geometry is simply described as bent without considering the nonbonding lone pairs. [citation needed] However, in liquid water or in ice, the lone pairs form hydrogen bonds with neighboring water molecules. The most common ...
Most molecules have lone pairs of electrons, which are sometimes stereochemically active. It is a matter of taste whether one includes the lone pair in a drawing. Lone pairs of electrons are more common for depictions that emphasize bonding, as in simple gaseous molecules, such as ammonia and nitric oxide.
This molecule has a ring with four sulfur atoms and two carbons, two ethane-1,1-dithiol molecules become linked at their sulfur atoms with the loss of hydrogen. [11] This can further oxidise to cis / trans -3,5-dimethyl-1,2,4-trithiolane which has a meat-like odour.
An atom bonded to 5 other atoms (and no lone pairs) forms a trigonal bipyramid with two axial and three equatorial positions, but in the seesaw geometry one of the atoms is replaced by a lone pair of electrons, which is always in an equatorial position. This is true because the lone pair occupies more space near the central atom (A) than does a ...