Draw the expected organic product from the reaction of 1-chloro-2,4-dinitrobenzene with CH3CH₂ON. Give detailed Solution with explanation needed with reaction. don't give Handwritten answer ! :☐
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- Cyclohexene reacts with bromine in the presence of NaI to yield -?Chemistry 60. Give the principal product(s) expected, if any, when trans-1,3-pentadiene reacts under the following conditions. Assume one equivalent of each reagent reacts unless noted otherwise. (a) H2O, H3O+ (b) Na+EtO- in EtOH (c) Maleic anhydride heatGive detailed Solution with explanation
- Please give the name of the compounds and explainReaction of -pinene with borane followed by treatment of the resulting trialkylborane with alkaline hydrogen peroxide gives the following alcohol. Of the four possible cis,trans isomers, one is formed in over 85% yield. (a) Draw structural formulas for the four possible cis,trans isomers of the bicyclic alcohol. (b) Which is the structure of the isomer formed in 85% yield? How do you account for its formation? Create a model to help you make this prediction.Question: Which of the following is the major product from bromination of meta-nitrobenzenesulfonic acid? * Br Br2 , FeBra heat NO2 or or or NO2 NO2 NO2 NO2 B. D. (A) (B) Question: C6H5OCH2CH2Br is heated with Mg in ether and then quenched in cold H2O. What organic product will be obtained ? * C6H50CH2CH3 C6H50CH2CH2OH C6H50H C6H6
- Predict the products of the following reactions.(a) sec-butyl isopropyl ether + concd. HBr, heat3) Draw equations of the following reactions and and explain to which direction is the respective quillibrium shifted. a) cyclohexylamine + water b) aniline + sulphuric acid c) triethylamine + acetic acidChoose which compound is more reactive when reacted with N2OH in water solvent and he reason clearly. vs OH HO,
- Possible alternative brominations include: Veratrole (1,2-dimethoxybenzene) to 1,2-dibromo-4,5-dimethoxybenzene; 4-Methylacetanilide to 2-bromo-4-methylacetanilide; 2-Methylacetanilide (made in experiment S.1) to 4-bromo-2-methylacetanilide; Vanillin to 5-bromovanillin; Acetanilide to 4-bromoacetanilide; a. b. C. d. e. EXPERIMENT S4: BROMINATION OF AROMATIC COMPOUNDS Certain other acetanilides made in experiment S.1 may also be used as precursors in this experiment. Estimated time: 1 afternoon Associated learning goals: Section 6, LG 6.6; Section 7, LG 7.2 and 7.4 Pre-lab report: complete the standard report form, and answer the following questions. In this experiment, molecular bromine (Br2) is generated from the redox reaction of potassium bromate with hydrobromic acid. Write a balanced equation for this process. Briefly outline the mechanism by which Br2 brominates your aromatic compound. Why do the bromine atoms end up at the positions indicated rather than anywhere else in the…G.267.What organic product would you expect from the reaction of ethylmagnesium bromide (CH3CH2MgBr) with the following reagent. then NH4CI, H2O Ph