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- Minor product via E1 for 2-butanol and HCl?select the most appropriate reagent(s) to effect the change. K2Cr2O7, H+ H2, Pd 1. Disiamylborane, 2. HO–, H2O, H2O2 NaOCl H2SO4, HgSO4Illustrate the resonance effect of the methoxy group -OCH3, on the structure of the benzene ring. Draw all the oissuvke resonance forms of methoxybenzene, including the hybrid Based on the structures, explain how the presence of the -OCH3 group affects: (i) the reactivity of the benzene ring towards electrophilic attack (ii) the orientation or point of attack of an incoming electrophilic reagent on the benzene ring.
- Why does naphthalene undergo electrophilic substitution at C1 instead of C2? Could you draw a structure for the intermediate that helps explain this?Please Could your help me for these questions 2, 3, 6. My reagents were 1-bromobutane and acetoneClassify following solvent as protic or aprotic CH3NO2
- Do a retrosynthetic analysis on the following compound, ending withavailable starting material.Perform a confirmational analysis on 2-bromo-3-methylbutane.Write TRUE if the statement is correct and FALSE if the statement is wrong. Please answer them all Substitution reactions do not occur in aromatic rings because of pi-electron delocalization. The resulting iodinated aspirin has a higher Rf compared to aspirin after visualizing with ferric chloride. The mobile phase used in determining the Rf of the iodinated aspirin is 5% ethyl acetate in acetic acid. When isopropyl alcohol reacts with HCI, the resulting product is 2-chloropropane. In Fehling's test, the theoretical product after an aldehyde is mixed with Fehling's Solution is alcohol. lodoform, which has a molecular formula of CH3l, is indicative that a ketomethyl group is present. Based on the physical property, hydroquinone has a lower boiling point compared to catechol. Picric acid, being a phenolic compound, tests positive for the FeCl3 test. Nucleophilic molecules are electron-rich molecules that can "attack" electron-deficient molecules. When FeCl3 is used in visualizing…
- A concerted, one-step reaction is involved between tert-Butyl bromide and sodium hydride at 50 o C.True or False?Help ASAP Illustrate the resonance effect of the methoxy group -OCH3, on the structure of the benzene ring. Do this by writing all the possible resonance forms for methoxybenzene, including the hybrid. Based on your structures, explain how the presence of the -OCH3 group affects: (i) the reactivity of the benzene ring towards electrophilic attack; (ii) the orientation or point of attack of an incoming electrophilic reagent on the benzene ring.1.Explain why pyridine ( Kb=2.3x10-9) is a much stronger base than pyrrole (Kb=2.5x10-14), 2.Explain and illustrate, why it is difficult to perfom Friedel-Craft reactions on unactivated pyridine.