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Despite its polarity, 2-chlorobutane is only slightly soluble in water due to the hydrocarbon chain its attached to, this makes it soluble in nonpolar-organic solvents. Like many alkyl halides, it is relativity reactive, although not as reactive as iodides and bromides (I>Br>Cl>F), because of this reactivity, alkyl fluorides are more stable ...
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
CH 2 =CHCO 2 H Propiolic acid: propynoic acid propargylic acid acetylene carboxylic acid CH≡CCO 2 H Lactic acid: 2-hydroxypropanoic acid milk acid CH 3 CHOHCO 2 H 3-Hydroxypropionic acid: 3-hydroxypropanoic acid hydracrylic acid CH 2 OHCH 2 CO 2 H Glyceric acid: 2,3-dihydroxypropanoic acid CH 2 OHCHOHCO 2 H Pyruvic acid: 2-oxopropanoic acid ...
(ch 3) 3 coh + hcl → (ch 3) 3 ccl + h 2 o Because tert -butanol is a tertiary alcohol, the relative stability of the tert -butyl carbocation in the step 2 allows the S N 1 mechanism to be followed, whereas a primary alcohol would follow an S N 2 mechanism.
tert-Amyl chloride (2-methyl-2-butyl chloride) is an alkyl chloride used for flavoring and odorizing. [2] At room temperature, it is a colorless liquid with an unpleasant odor. It is an isomer of 1-chloropentane ( n -amyl chloride).
H 2 C=CH 2 + HCl → CH 3 CH 2 Cl. In oxychlorination, hydrogen chloride instead of the more expensive chlorine is used for the same purpose: CH 2 =CH 2 + 2 HCl + 1 ⁄ 2 O 2 → ClCH 2 CH 2 Cl + H 2 O. Secondary and tertiary alcohols react with hydrogen chloride to give the corresponding chlorides.
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1-Chlorobutane is an alkyl halide with the chemical formula CH 3 (CH 2) 3 Cl. It is a colorless, flammable liquid. It is a colorless, flammable liquid. Preparation and reactions