enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Boiling points of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Boiling_points_of_the...

    H 2 20.271 K (−252.879 °C) ... Am 2880 K (2607 °C) Cm 3383 K (3110 °C) Bk 2900 K ... Primordial From decay Synthetic Border shows natural occurrence of the element.

  3. Potassium ozonide - Wikipedia

    en.wikipedia.org/wiki/Potassium_ozonide

    6 KOH + 4 O 3 → 4 KO 3 + 2 KOH(H 2 O) + O 2. The compound is metastable, and will decompose to potassium superoxide and oxygen, especially if there is any water in the atmosphere. Long-term storage in very dry atmosphere is possible below around 0 °C. [3] KO 3 → KO 2 + ½ O 2. This compound reacts with water to form potassium hydroxide and ...

  4. Tetramethyl orthosilicate - Wikipedia

    en.wikipedia.org/wiki/Tetramethyl_orthosilicate

    Tetramethyl orthosilicate (TMOS) is the chemical compound with the formula Si(OCH 3) 4.This molecule consists of four methoxy groups bonded to a silicon atom. The basic properties are similar to the more popular tetraethyl orthosilicate, which is usually preferred because the product of hydrolysis, ethanol, is less toxic than methanol.

  5. Hammett equation - Wikipedia

    en.wikipedia.org/wiki/Hammett_equation

    Reactivity of 4-substituted bicyclo[2.2.2]octane-1-carboxylic acids and esters were measured in 3 different processes, each of which had been previously used with the benzoic acid derivatives. A plot of log(k) against log(K A) showed a linear relationship.

  6. Infrared spectroscopy correlation table - Wikipedia

    en.wikipedia.org/wiki/Infrared_spectroscopy...

    cis-1,2-disub. alkenes 1660 medium trans-1,2-disub. alkenes 1675 medium trisub., tetrasub. alkenes 1670 weak conjugated C═C dienes 1600 strong 1650 strong with benzene ring 1625 strong with C═O 1600 strong C═C (both sp 2) any 1640–1680 medium aromatic C═C any 1450 weak to strong (usually 3 or 4) 1500 1580 1600 C≡C terminal alkynes

  7. Trimethyl borate - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_borate

    Trimethyl borate is the main precursor to sodium borohydride by its reaction with sodium hydride in the Brown-Schlesinger process: . 4 NaH + B(OCH 3) 3 → NaBH 4 + 3 NaOCH 3. It is a gaseous anti-oxidant in brazing and solder flux.

  8. Trimethyl phosphite - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_phosphite

    P(OCH 3) 3 → CH 3 P(O)(OCH 3) 2. As a ligand, trimethyl phosphite has a smaller cone angle and better acceptor properties relative to trimethylphosphine. A representative derivative is the colorless tetrahedral complex Ni(P(OMe) 3) 4 (m.p. 108 °C). [4] The tridentate ligand called the Kläui ligand is derived from trimethyl phosphite. The ...

  9. Trimethyl orthoformate - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_orthoformate

    Trimethyl orthoformate is a useful building block for creating methoxymethylene groups and heterocyclic ring systems. It introduces a formyl group to a nucleophilic substrate, e.g. RNH 2 to form R-NH-CHO, which can undergo further reactions.

  1. Related searches och3 shows m or cm x h 2 k solve for k 8

    och3 shows m or cm x h 2 k solve for k 8 plusy=(x-h)^2 k