Predict the major products of bromination of the following:
a)toulene b)nitrobenzene c)benzaldehyde d)benzoic acid?
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Predict the major products of bromination of the following compounds a) Toluene c) Nitrobenzene b) Bromobenzene d) Anisole c) Acetophenone
1. Predict the major products formed when benzene reacts with the following reagents. (a). tert-butyl bromide, ALCl3 (b) bromine + a nail (c) iodine + HNO3 (d) carbon monoxide, HCl, and AlCl3/CuCl (e) nitric acid + sulfuric acid. 2. Predict the major products of the following reactions. (a.) nitrobenzene + ethyl chloride/AlCl3 (b). p-methylanisole + acetyl chloride + AlCl3 (c). nitrobenzene + fuming sulfuric acid (d) benzene + CH3CH2COCl in the presence of (1) ALCl3 followed by...
Study Pr 3 Predict the major products of the following reactions. (a) 2,4-dinitrochlorobenzene + NaOCH3 (c) nitrobenzene + fuming sulfuric acid (e) p-methylanisole + acetyl chloride AICI, (g) 1,2-dichloro-4-nitrobenzene NaNH2 (i) p-ethyibenzenesulfonic acid +steam/H (b) phenol + tert-butyl chloride + AICl, (d) nitrobenzene + acetyl chloride +AlC1 (f) p-methylanisole + Br2, light (h) p-nitrotoluene + Zn + dilute HCl j) p-ethylbenzenesulfonic acid + HNO3, H2S + hot, concd. KMnO Ph-C-NHPh + CH,CH,-C-CI, AICI3 indane Study Pr 3 Predict the major...
all steps of bromination 2 Write the mechanism for the following radical reaction. Predict the products. Once products are predicted, circle which one is the major product and why? (10) Brzo ? UV light
1. Bromination of an alkene is restricted to a syn addition. In this problem you will design an experiment to validate or provide evidence that alkene bromination undergoes syn addition You will use the following starting alkene a) trans-stilbene b) cis-stilbene A. Draw the mechanisms showing all electron flows (curved arrows) and the cyclic halonium intermediate to predict the stereochemical products of the bromination reaction for (a) trans-stilbene and (b) cis-stilbene formed from syn addition. B. Design the experiment to...
Need help understanding. Thanks! 15. Which of the following structures is the most important contributor to the resonance hybrid formed as intermediate when aniline undergoes para-bromination? NH2 NH2 NH2 Br D 16. Select the product of the following reaction H2 Pd/C NO2 Он Он NH2 NO2 NO2 NH2 A. В. C. D. 17. What is the starting material in the reaction below? 1. Mg cон 2. CO2 then acid A. Bromobenzene B. Benzyl bromide C. Benzoic acid D. Lithium benzoate...
!!! If each compound undergoes electrophilic aromatic substitution, where should the substituent be added? *The choices for each are either ortho/para position OR meta position.* Phenol? Benzaldehyde? Benzoic Acid? Bromobenzene? Nitrobenzene? Toluene?
Predict the major bromination product of the following compounds using Br2/FeBr3 in the dark. Explain your answers. a) b) c) OMe OMe OMe
Electrophilic bromination of an equimolar mixture of methylbenzene (toluene) and (trifluoromethyl)benzene with one equivalent of bromine gives exclusively 1-bromo-2-methylbenzene and 1-bromo-4-methylbenzene. Explain why none of the (trifluoromethyl)benzene reacts Explain the regiochemical outcome of the reaction In other words, why are 1-bromo-2-methylbenzene and 1-bromo-4-methylbenzene formed from the toluene? Electrophilic nitration of benzoic acid gives almost exclusively 1,3-nitrobenzoic acid. By drawing the appropriate resonance forms of the intermediate cations resulting from attack of [NO2]+, explain this result.
What is the expected major product resulting from the reaction of benzaldehyde with potassium permanganate? Select one: a. benzoic acid b. benzyl alcohol c. methylbenzene d. cyclohexanone e. no reaction