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- 2. Write a complete mechanism for the reaction shown below, including how the electrophile is generated. HNO3 H2SO4 NO2Major product and mechanism for this reaction?In EAS bromination reactions, a -CON(CH3)2 substituent on the aromatic ring is: an activator and an o,p-director. a deactivator and a m-director. an activator and a m-director. the substituent catalyzes the 1,2 addition of bromine across the double bond. a deactivator and an o,p-director. G
- Complete the reaction map by matching A-E with the given choices. H2 H2 B E Pt Cla Na in lig NH3 он + но Match each item to a choice A3A Complete the reactions below. H₂SO4/H₂O HgSO4 A NaBH4 EtOH B лH₂SO4 C10:54 ← Question 21 of 32 Draw the major product of this reaction. Ignore inorganic byproducts. Submit Assume that the water side product is continuously removed to drive the reaction toward products. (CH3)2NH, TSOH Select to Draw | I I
- Complete the following reactions: indicate the mechanism (SN1 or SN2). If the reaction does not proceed, indicate so and the reason as to why it would not.Will the following bases favor an E1 or E2 mechanism? H2O, CH3CO2^-, tBuO^-, CH3CH2OH, -NH2, NaHMatch the reactant with the product of its reaction with HClO4. Leave blank if there is no reaction. Group of answer choices K2S KHCO3 HNO3 K2SO3
- Major product and mechanism for this?Rank the following compounds in order of increasing reactivity in a substitution reaction with −CN as nucleophile.In both examples below the reactants shown are combined to bring about a nucleophilic substitution (Sy1, Sy2) and/or elimination (E1, E2) reaction. What is the major reaction that takes place in each case? CI CH2CI NaOH H20 SN2 E2 mixture of SN1 and E1 CH3 CI CH3OH CH3