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Anhydrous solvents are commercially available from chemical suppliers, and are packaged in sealed containers to maintain dryness. [4] Typically anhydrous solvents will contain approximately 10 ppm of water and will increase in wetness if they are not properly stored. Organic solutions can be dried using a range of drying agents.
A-type granite is a particular category of the S-I-A-M or 'alphabet' system which classifies granitoids and granitic rock by their photoliths or source. [1] [2] The 'A' stands for Anorogenic or Anhydrous, as these granites are characterized by low water content and a lack of orogenic or transitional tectonic fabric. [3]
A solution of a carbonyl compound is added to a Grignard reagent. (See gallery) An example of a Grignard reaction (R 2 or R 3 could be hydrogen). The Grignard reaction (French:) is an organometallic chemical reaction in which, according to the classical definition, carbon alkyl, allyl, vinyl, or aryl magnesium halides (Grignard reagent) are added to the carbonyl groups of either an aldehyde or ...
Because acetic anhydride is not stable in water, the conversion is conducted under anhydrous conditions. To a decreasing extent, acetic anhydride is also prepared by the reaction of ketene with acetic acid at 45–55 °C and low pressure (0.05–0.2 bar). [8] H 2 C=C=O + CH 3 COOH → (CH 3 CO) 2 O (ΔH = −63 kJ/mol)
The presence of water in the reaction mixture has been shown to have a significant effect on enantiomeric excesses, and thus the CBS reduction must be conducted under anhydrous conditions. [14] Temperature also plays a critical role in the observed stereoselectivity. In general, at lower temperatures enantiomeric excesses (ee's) are obtained.
Since acyl chlorides and acid anhydrides also react with water, anhydrous conditions are preferred. The analogous acylations of amines to give amides are less sensitive because amines are stronger nucleophiles and react more rapidly than does water. This method is employed only for laboratory-scale procedures, as it is expensive.
The Suzuki reaction or Suzuki coupling is an organic reaction that uses a palladium complex catalyst to cross-couple a boronic acid to an organohalide. [1] [2] [3] It was first published in 1979 by Akira Suzuki, and he shared the 2010 Nobel Prize in Chemistry with Richard F. Heck and Ei-ichi Negishi for their contribution to the discovery and development of noble metal catalysis in organic ...
Such compounds must be prepared in anhydrous conditions, since the nitrate ion is a much weaker ligand than water, and if water is present the simple nitrate of the hydrated metal ion will form. The anhydrous nitrates concerned are themselves covalent, and many, e.g. anhydrous copper nitrate, are volatile at room temperature. Anhydrous titanium ...