In each of the following reactions, the aromatic ring has just one chemically distinct, aromatic H,...
Electrophilic Aromatic Substitution: Reagents 1. Each of the following transformations can be carried out in one or two steps. Fill in the reagents required for each step. If a second step is not needed, please put an "X" through the second box 2. CI 2. OH 2. CH, CHE SO,H 2. 2.
Benzene will engage in electrophile aromatic substitution reactions. Which of the following statemtns is NOT TRUE about the mechanism for this reaction? please help I dont know what to put! 3. Benzene will engage in electrophilic aromatic substitution reactions. Which of the following statements is not true about the mechanism for this reaction? A. Formation of a carbocation intermediate is the rate-determining step. B. The carbocation intermediate has an sp3-hybridized carbon in the ring. C. Benzene is an electrophile. D....
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
Predict whether the following molecules are aromatic, antiaromatic, or non aromatic and explain why: o non armannot conjugated Predict the reagents (a)/products (b) for the following transformations: SO, H.SO HNO AICI, HESO Oxidize to break aromahcity Foclo Cly radical Predict the relative ratios (major, minor) of the following products in these electrophilic aromatic substitution reactions by drawing the mechanism for the formation of each product and identifying important intermediates to describe relative stability:
1. please check what is wrong. Thank you! Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
please help in all sections asap!! Provide the reagents necessary to carry out the following conversion. NO Br Choose the correct reagents for step 1. fuming H2SO4 Br2/ FeBr3 HNO3/ H2SO4 CH3Br / FeBr3 Choose the correct reagents for step 2 HNO3/ H2SO4 CH3Br/ FeBr3 fuming H2SO4 Br2/ FeBry Which one of the following substituents will direct the incoming group to the meta position during electrophilic aromatic substitution? -NO2 -CEN -CCl -COOH all of these O O Identify the electrophile...
The following four reactions show reactants, reagents, and products. In each reaction one of the categories is missing. Supply the missing compound or reagents in each of the reactions. Be sure to indicate stereochemistry where warranted.
2. Which one of the following compounds is more reactive towards Electrophilic Aromatic Substitution? PhCO,H PhCCI, PhCN PhCHE PhCI A B с D E
please only box one answer for each of these questions. HOH • SOCI + SO, HC a = Proton transfer b = Lewis acid base c = Radical chain substitution d = Radical chain addition e = Electrophilic addition f= E1 Elimination g = E2 Elimination h = Syl Nucleophilic substitution = Sy2 Nucleophilic substitution = Electrophilic aromatic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters - for...
aromatic reactivity mechanisms not needed only products Draw the product(s) of the following reactions HNO/H,SO AICI SOY/H2SO4 Bry/FeBry HNO/H,80 AICI Bry/FeBry