1) Arrange the assigned benzene substituents in order of reactivity in EAS reactions. Explain the trend...
Name: TA: Partner: 1) Arrange the assigned benzene substituents in order of reactivity in EAS reactions. Explain the trend (1.5 points) 2) Use your knowledge of resonance, aromaticity, and general stability trends to analyze the following sets of reactions, explain why each reaction is fast or slow (1.5 points) CH3OH CH3OH fast slow + Br Lab 6! Chemistry Of Aromatic Compounas Part 2: 2) Starting with a compound with 6 (or less carbons) propose a synthesis for the assigned compounds....
1) Arrange the assigned benzene substituents in order of reactivity in EAS reactions. Explain the trend (1.5 points) pro mo ph Ph-M Ph-8
Name: TA: Partner: 1) Arrange the assigned benzene substituents in order of reactivity in EAS reactions. Explain the trend (1.5 points) Ph-sv PAN
1) Classify the molecules below as aromatic, anti-aromatic, or non-aromatic. (1 points) 2) Use your knowledge of resonance, aromaticity, and general stability trends to analyze the following reaction provide your reasoning why that reaction is fast or slow (1 point) Reasoning: NaNH2 slow Lab 6: Chemistry of Aromatic Compounds pka = 36 NaNH2 fast pka = 16 CHE 202 Sp 2020-Lab 6-AART 1 (5 points): GROUP WORK
Predict the relative order of reactivity of the indicated carbonyl compounds in reactions with nucleophiles (1 = most reactive carbonyl electrophile). Use all three logic arguments of organic chemistry (resonance, inductive and steric). Show structures, lone pairs and arrow-pushing conventions in your answer to provide an explanation for your order of reactivity. Write the expected product in a reaction with lithium aluminium deuteride, LiAlD4, followed by workup (no mechanisms) Name 2. Predict the relative order of reactivity of the indicated...
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:...