Name the major organic product which results when benzenesulfonic acid reacts with Cl2 in AICI3, followed by heating the compound in a NaOH in H2O to 350 C and finally heated in aqueous acid. 1. Cl/AICI3 S-OH 2. NaOH/H2O at 350 °C benzenesulfonic acid 3. dilute H30*
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- Pls solve this question correctly in 5 min i will give u like for sure Balance the chemical equation of a reaction formed by the bromination of trans-cinnamic acid if we started with 0.3088 grams of trans cinnamic acid and 1mL of bromine. The product of this reaction is 2,3 - dibromo - 3- phenylpropanoic acidTunicates are marine animals that are called "sea squirts" because when they are taken out of water, they tend to contract and expel seawater. Lepadiformine is a cytotoxic agent (toxic to cells) isolated from a marine tunicate. During a recent synthesis of lepadiformine, the investigators observed the formation of an interesting by-product (3) while treating diol 1 with a reagent similar in function to PBr3 (J. Org. Chem. 2012, 77, 3390–3400):Assuming a 56.8% yield, how kany ml of alkene is required to produce 22.5 mL of 2,3-dimethyl-2-butanol? MW of alkene: 84.16, d: 0.653 MW of 2,3-dimethy-2-butanol: 102.17, d:0.823
- Fill in necessary products reactants or reagants of these reactions. Please note the existence of enantionmers in some cases.During an acid base extraction of an organic compound dissolved in dichloromethane with sodium bicarbonate (NaHCO3), you do not recover any of the desired extracted product after completing all the remaining steps. What could the most probable reason(s) be for the observed outcome? -The organic compound you want to extract is also a base; an acid is needed -You did not degassed/vent the separatory funnel -You did not shake the separatory funnel enough to react the base with the organic compound -You did not heat the mixture before the extraction -The organic compound evaporate from separatory funnel during the extractionWhich of the following statements is not correct? Oxymercuration-demercuration for alcohol synthesis is complicated by carbocation rearrangement. Oxymercuration-demercuration for alcohol synthesis follows Markonikov's Rule. Sodium borohydride is used in the last step of oxymercuration-demercuration to oxidize the hydroxyalkyl mercury compound. All of the above. Both the 1st and the 3rd statements.
- 22- Give one example for the hydration of Alkene: That is the Addition of H2O byoxymercuration. Give the proper Mechanism if possible.23- Give one example for the hydration of Alkenes: that is: the addition of H2O byHydroboration.E. TESTS FOR PHENOLIC COMPOUNDSPhenolic compounds such as phenol, salicylic acid, etc., give characteristiccolors with FeCl3 and Millon’s Reagent.1. Ferric Chloride TestAdd 5 drops of FeCl3 solution to 4 different test tubes containing 1 mL each ofdilute solutions of the following compounds and note the color obtained.a. Phenol _______________________________________________________________b. Salicyclic acid ___________________________________________________________c. Resorcinol _______________________________________________________________d. Picric acid _______________________________________________________________2. Millon’s TestPrepare another set of 4 test tubes containing 1 mL each of the solutions listedbelow. Add 3 drops of Millon’s reagent to each and place all the test tubes in aboiling water bath. Note the color formed.a. Phenol _______________________________________________________________b. Salicylic acid ___________________________________________________________c.…In which of the statements given below, the event is not an oxidation reaction? A. Product formation as a result of the reaction of benzoine with nitric acid B. Formation of the product as a result of the reaction of 2-propene at KMnO4 / Basic ambient temperature C. Formation of the product as a result of the reaction of 2-propene in KMnO4 / Basic medium cold D. CH3CH2OH + KMnO4 → CH3COOH E. Reaction of an alkyl halide with ammonia
- CH₂ + Using the reagents below, list in order (by letter, no period) those necessary to prepare 2-butyne from acetylene. Note: Not all spaces provided may be needed. Type "na" in any space where you have no reagent. a. Br₂, heat, light b. Na, (-H₂) c. Nal(SN2) d. NH4NO3 e. 1) NaNH2, liq. NH3, 2) CH3Br f. (CH3)3COK, (CH3)3COH, heat g. NaOEt, EtOH, heat Step #1 Step #2 Step #3I am trying to calculate the theoretical & actual percent yield of amyl acetate from a Fischer reaction of 1-pentanol, H2SO4, and acetic anhydride. The final product obtained was 28.7g. Here is the information I know: 29mL of acetic anhydride was used, 5mL of H2SO4 was used as a catalyst, and (0.24mol) 26mL of 1-pentanol was used.SHOW COMPLETE SOLUTIONS Q3. Which isolate has A260/280 ratio of above 2.0?