The answer could be 2 if we did the monochlorination of cyclohexene instead. 1. Question: Monochlorination Of N-hexane Gives A Mixture Of 1-chlorohexane, 2-chlorohexane And 3-chlorohexane. CH3 side chains. & [18] The current n-hexane PEL in the US is 500 ppm (1,800 mg/m3 (0.79 gr/cu ft)). Answered Monochloronation of n-hexane 2 See answers Wendy16 is waiting for your help. Assume The Secondary Hydrogens In Hexane Are Equally Reactive To Monochlorination, What Is … Like gasoline, hexane is highly volatile and is an explosion risk. Commercial hexane is a solvent consisting of six-carbon isomers principally n-hexane (53%), 3-methyl pentane (16%), methylcyclopentane (14%), and 2-methyl pentane (12%). 4 CHs.
Wendy16 Wendy16 8 minutes ago Chemistry Secondary School +5 pts. Log in. [13], The acute toxicity of hexane is rather low. The term hexanes refers to a mixture, composed largely (>60%) of hexane, with varying amounts of the isomeric compounds 2-methylpentane and 3-methylpentane, and, possibly, smaller amounts of nonisomeric C5, C6, and C7 (cyclo)alkanes. It is slowly being replaced with other solvents.[20]. > They are (Chloromethyl)cyclohexane 1-Chloro-1-methylcyclohexane 1-Chloro-2-methylcyclohexane 1-Chloro-3-methylcyclohexane 1-Chloro-4-methylcyclohexane They are diastereomers, 'stereoisomers that are not mirror images'. Cloudflare Ray ID: 5ecab6f30e2d087b
Monochlorination of an alkane involves substituting one of the hydrogens in the alkane with a chlorine atom. Higher alkanes present as impurities in hexanes have similar retention times as the solvent, meaning that fractions containing hexane will also contain these impurities. It is a colorless liquid, odorless when pure, and with boiling points approximately 69 °C (156 °F). In organic chemistry, free-radical halogenation is a type of halogenation.This chemical reaction is typical of alkanes and alkyl-substituted aromatics under application of UV light.The reaction is used for the industrial synthesis of chloroform (CHCl 3), dichloromethane (CH 2 Cl 2), and hexachlorobutadiene.It proceeds by a free-radical chain mechanism. The industrial product (usually around 50% by weight of the straight-chain isomer) is the fraction boiling at 65–70 °C (149–158 °F). Of the five isomeric hexanes , the isomer which can give two monochlorinated compounds, is (a) 2-methylpentane (b) 2,2-dimethylbutane (c) 2,3-dimethylbutane Thus, monochlorination of propane will lead to 2 products. Allowing dichlorination gives more than just three products - due to both geometrical and optical isomerism. You may need to download version 2.0 now from the Chrome Web Store. • If you are on a personal connection, like at home, you can run an anti-virus scan on your device to make sure it is not infected with malware. Hexanes is cheaper than hexane and is often used in large scale operations not requiring a single isomer (e.g., as cleaning solvent or for chromatography). Whereas, in case of cyclohexane, all the hydrogen atoms are equivalent to 2o. In preparative chromatography, concentration of a large volume of hexanes can result in a sample that is appreciably contaminated by alkanes. Should you stop eating veggie burgers? The formula for 3,4-dimethyl hexane is: CH3-CH2-CH-CH-CH2-CH3.....CH3 CH3. Completing the CAPTCHA proves you are a human and gives you temporary access to the web property. Therefore, chlorination of cyclohexane leads to the formation of same product : chlorocyclohexane. Currently, as it stands, the answer 3 is wrong. By way of example consider the monochlorination of propane: CH3-CH2-CH3 + Cl2 -----> ?
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