6. Identify the most likely mechanism and identify the products aromatic substitution reactions. of the following nueleophilic Ci 1) NaOH, 350°C 2) HCl, H20 1) NaNH2 1) NaOH, 350 °C 2) HCI, H20...
show the mechanism for these reactions Br Br Pd/C Br2 Br ?? Br, H20 HCI CI Br ?? H2O+
1. Predict the products of the following reactions. excess NaNH2 THE Br Br H 1. NaNH2 2. CH3CH,Br H2SO4, H20 Hz, Pd/BaSO4 quinoline, CH3OH Na, NH3 1 equivalent HBO NaNH2 Br (excess) 1. Sia,BH, THE 2. H2O2, NaOH HgSO4 H2SO4 H2O
For each of the following substitution reactions, use the available information to identify the one, most likely mechanism (SN1 vs. SN2), then draw all of the predicted products (labeling major/minor products as necessary). Be sure to provide adequate justification for your responses. 3. но warm Ci a. CH3ONa CH3OH Br b. 4. Draw a step-by-step mechanism that accounts for the following SN1 reaction: CI CH3CH2OH warm OCH2CH3
Complete the following reactions. phenol CI Br hhalimide, NaOH 2) NaOH/H20, Heat 1) NaOH 2) H30* H2o CH 1) NaN2 2) 3) H20
1. Li 2. aq. NaOH reflux Cl NaCI+H20 a Proton transfer b Lewis acid/base c E2 elimination d SN2 Nucleophilic substitution e-Electrophilic aromatic substitution f Carbonyl nucleophilic addn g Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1. 2. 1.8% Hyc's、CH, + H CH3 2. N(CHs CI a Proton transfer b-Lewis acid/base E2...
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:...
4.2 Give a detailed mechanism and show the products of the following reactions: OF CH3 C (6] a) C-H E2 ООCH H CHз H b) H3CC E1 CH3 Н-О Br 4.3 Label the following reactions as SN1, SN2, E1, or E2. . Br NaNH2 THE a) HN CI КОН Ethanol b) но Ethanol c) NaOH Ethanol P OH 4A samnle with a.concentration of 0 3 a/ml was nlaced in a cell with a lenath of 5 cm 41
Predict the products of the following reactions 1 equivalent HBr NaNH2 Br (excess) 1. Sia BH, THE 2. H2O2, NaOH HgSO4 H2SO4 H20
VOX Homework 6 - Chapter 6 1. Predict the products of the following reactions. excess NaNH2 THF Br Br H 1. NaNH, 2. CH CH Br H2SO4 H20 ♡ SOHO H2, Pd/BaSO4 quinoline, CH3OH Na, NH3
Help! 1. 1. LIAIH4 / dry ether он 2. aqueous H2S04 2. AICl3 Ci но dSN2 Nucleophilic substitutiong a = Electrophilic addition b E2 Elimination c SN1 Nucleophilic substitution f Carbonyl nucleophilic addn g = Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn Electrophilic aromatic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -i for your answers. 2. Review Topics] 1. HCI reflux он +...