Get more help from Chegg. This reagent can be used, e.g. [4] Little is known about chronic effects.

Bromobenzene and magnesium form benzoic acid in a 1:1 mol ratio. Part 1 out of 2 Bromobenzene is prepared by the action of bromine on benzene in the presence of Lewis acid catalysts such as ferric bromide.. Bromobenzene is used to introduce a phenyl group into other compounds.

The numbers you've provided would imply that magnesium is the limiting reagent as there are fewers moles magnesium compared to bromobenzene. Synthesis and reactions. in the reaction with carbon dioxide to prepare benzoic acid. Chloroacetate + Cyclohexanone, + Chlorobenzene, + Bromobenzene, or + Benzyl Alcohol at (298.15, 303.15, and 308.15) K". [3] Other methods involve palladium-catalyzed coupling reactions such as the Suzuki reaction. It is a colourless liquid although older samples can appear yellow. Post your questions about chemistry, whether they're school related or just out of general interest. For Bromobenzene: 0.70mL bromobenzene * (1.495g/mL) *(1 mol / 157.01g) = 0.00667 mol bromobenzene For Magnesium: 0.15g Mg * (1 mol / 24.3 g) = 0.00617 mol Mg. Please do not post entire problem sets or questions that you haven't attempted to answer yourself. Bromobenzene is prepared by the action of bromine on benzene in the presence of Lewis acid catalysts such as ferric bromide. Bromobenzene is used to introduce a phenyl group into other compounds. in the reaction with carbon dioxide to prepare benzoic acid. I'm confused because everyone else is saying that the bromobenzene is the limiting reagent. Press question mark to learn the rest of the keyboard shortcuts.

Animal tests indicate low toxicity. I would check to make sure that your starting amounts are correct and after that I would ask to see someone else's calculations so you can see why you are getting a different result compared to them; worry less about what result they got and more about how they got it. One method involves its conversion to the Grignard reagent, phenylmagnesium bromide. One method involves its conversion to the Grignard reagent, phenylmagnesium bromide.This reagent can be used, e.g. The numbers you've provided would imply that magnesium is the limiting reagent as there are fewers moles magnesium compared to bromobenzene. Journal of Chemical & Engineering. the 122.12 g/mol is the molar mass of benzoic acid. [7], Except where otherwise noted, data are given for materials in their, "IFA - Databases on hazardous substance (GESTIS): GESTIS database on hazardous substances", https://en.wikipedia.org/w/index.php?title=Bromobenzene&oldid=936809883, Pages using collapsible list with both background and text-align in titlestyle, Articles containing unverified chemical infoboxes, Creative Commons Attribution-ShareAlike License, This page was last edited on 21 January 2020, at 03:42. I just checked the lab book again and the numbers are correct.

You should be putting your reagents in terms of mols; you can't compare grams of one substance to grams of another. Make pentane from butane c. Make tert-butyl alcohol from butane d. Make formaldehyde from methane. Bromobenzene is used as a precursor in the manufacture of phencyclidine. Benzyl alcohol can be synthesized from bromobenzene and simple organic/inorganic reagents.

Bromobenzene is an aryl halide, C6H5Br. Draw the compounds to show how benzyl alcohol can be synthesized. [5][6], For liver toxicity, the 3,4-epoxide are proposed intermediates.



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