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- Draw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent. excess CH3IWhich electrophile is most likely to undergo a 1,2-hydride shift during an electrophilic aromatic substitution reaction with benzene and AICI3? CI CI CI CIIdentify the lettered compounds in each reaction sequence.Draw the product formed when phenylacetonitrile (C6H5CH2CN) istreated with below reagent. H3O+
- Draw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent. CH3COCl, AlCl3Which of the following reactions describes why Acetic Anhyhdride needs to stay dry in order for it to be used in a Freidel Crafts Acylation? A + H20 H;C он H3C CH3 OH B + H20 H3C C .CH3 H;C CH3 + H20 H3C both A and B are side reactions that can scavenge waterIdentify the lettered compounds in each reaction sequence.Draw the product formed when phenylacetonitrile (C6H5CH2CN) istreated with below reagent. H2O, −OH
- Which of the following can cyclize to form the hemiacetal shown? A. O= B. H+ OH с. Хон фахран дархан OH OH D. OHThe products of acidic cleavage of Ethyl isopropyl ether by Hl are: O Al Isopropyl iodide and Ethanol Bi lsapropanol and lodoethane CHisopropane and Ethane DI Mixture of both A and BThe treatment of isoprene [CH2 = C(CH3)CH = CH2] with one equivalent of mCPBA forms A as the major product. A gives a molecular ion at 84 in its mass spectrum, and peaks at 2850–3150 cm−1 in its IR spectrum. The 1H NMR spectrum of A is given below. What is the structure of A?
- Search a reaction scheme for each reaction and draw the step-by-step mechanism using curved arrows for the following reactions. Explain how the IR spectrum (IR peaks of the functional groups) of the product would differ from that of the reactant in each reaction Grignard reaction Reduction of aldehydes or ketones Acetal or Ketal formation Wittig reactionRank the compounds in each group in order of increasing reactivity in nucleophilic acyl substitution. CH3CH2CO2H, (CH3CH2CO)2O, CH3CH2CONHCH3O -NHCCH3 CH₂CH3 ELECTROPHILIC AROMATIC SUBSTITUTION IN ARYLAMINES CH3C O - NHCCH3 0 CH₂CH3