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The energy released by the solvation of the ammonium ions and nitrate ions is less than the energy absorbed in breaking up the ammonium nitrate ionic lattice and the attractions between water molecules. Dissolving potassium hydroxide is exothermic, as more energy is released during solvation than is used in breaking up the solute and solvent.
Preshave products and some shave creams contain potassium hydroxide to force open the hair cuticle and to act as a hygroscopic agent to attract and force water into the hair shaft, causing further damage to the hair. In this weakened state, the hair is more easily cut by a razor blade. Potassium hydroxide is used to identify some species of ...
An even better (lower-cost and environmentally friendlier) process of making methanesulfonic acid was developed in 2016 by Grillo-Werke AG (Germany). It is based on a direct reaction between methane and oleum at around 50 °C and 100 bar in the presence of a potassium persulfate initiator.
An alcohol solution of potassium hydroxide decomposes it to potassium chloride and potassium carbonate in water: [11] CCl 4 + 6 KOH → 4 KCl + K 2 CO 3 + 3 H 2 O. Carbon is sufficiently oxophilic that many compounds react to give phosgene:
The complete removal of the water is critical for the reaction conversion, due to the pronounced hygroscopy of potassium hydroxide, which contains about 10% of water. [3] The significantly higher dissolution rate of potassium hydroxide in methanol compared to sodium hydroxide is advantageous.
In this motif the positions of the anions and cations are reversed relative to their positions in CaF 2, with potassium ions coordinated to 4 oxide ions and oxide ions coordinated to 8 potassium. [6] [7] K 2 O is a basic oxide and reacts with water violently to produce the caustic potassium hydroxide.
A neutralization reaction is a type of double replacement reaction. A neutralization reaction occurs when an acid reacts with an equal amount of a base. This reaction usually produces a salt. One example, hydrochloric acid reacts with disodium iron tetracarbonyl to produce the iron dihydride: 2 HCl + Na 2 Fe(CO) 4 → 2 NaCl + H 2 Fe(CO) 4
Dichlorocarbene is an intermediate in the carbylamine reaction. In this conversion, a dichloromethane solution of a primary amine is treated with chloroform and aqueous sodium hydroxide in the presence of catalytic amount of the phase-transfer catalyst. Illustrative is the synthesis of tert-butyl isocyanide: [7]