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2-Bromoanisole is an organobromide with the formula BrC 6 H 4 OCH 3. A colorless liquid, it is one of three isomers of bromoanisole, the others being 3-bromoanisole and 4-bromoanisole . It is a standard coupling partner in metal catalyzed coupling reactions.
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
In chemistry, a phenol ether (or aromatic ether) is an organic compound derived from phenol (C 6 H 5 OH), where the hydroxyl (-OH) group is substituted with an alkoxy (-OR) group. Usually phenol ethers are synthesized through the condensation of phenol and an organic alcohol ; however, other known reactions regarding the synthesis of ethers can ...
Anisole undergoes electrophilic aromatic substitution reaction at a faster speed than benzene, which in turn reacts more quickly than nitrobenzene.The methoxy group is an ortho/para directing group, which means that electrophilic substitution preferentially occurs at these three sites.
This can also explain why phosphorus in phosphanes can't donate electron density to carbon through induction (i.e. +I effect) although it is less electronegative than carbon (2.19 vs 2.55, see electronegativity list) and why hydroiodic acid (pKa = -10) being much more acidic than hydrofluoric acid (pKa = 3).
2.65 5.5 –5.12 K b & K f [2] Bromobenzene: 1.49 156.0 6.26 –30.6 Camphor: 204.0 5.95 179 –40 K f [2] Carbon disulfide: 1.29 46.2 2.34 –111.5 –3.83 Carbon tetrachloride: 1.58 76.8 4.88 –22.8 –29.8 K b & K f [1] Chloroform: 1.48 61.2 3.88 –63.5 –4.90 K b & K f [1] Cyclohexane: 80.74 2.79 6.55 –20.2 Diethyl ether: 0.713 34.5 2. ...
The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol . This reaction was developed by Alexander Williamson in 1850. [ 2 ] Typically it involves the reaction of an alkoxide ion with a primary alkyl halide via an S N 2 reaction .
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