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) Ph-sv PAN
1) Arrange the assigned benzene substituents in order of reactivity in EAS reactions. Explain the trend (1 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 points) CH3OH CH3OH fast slow 2) Starting with a compound with 6 (or less carbons) propose a synthesis for the assigned compounds. Provide all reagents and show intermediates (2 points) | 4) Provide all the...
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....
Arrange the following in order of decreasing reactivity towards hydrolysis using aqueous NaOH and explain this trend. (1.5) (a) CH3CO2CH3 (b) CH3COCI (c) CH3CON(CH3)2 (d) CH3CO2COCH3
1. arrange the halides in order of reactivity under the two sets of conditions Part 2: A Comparison of the Reactivity of Alkyl Halides 2% ethanolic silver nitrate 15 Nal in acetone 1. n-butyl chloride Clear Milky precipitate 2. sec-butyl chloride After heating, some precipitation 3. t-butyl chloride White precipitate After heating, precipitate Clear No precipitate Milk precipitate 4. n-butyl bromide Clear 5. allyl chloride White precipitate Brown color precipitate 6. chlorobenzene Clear Clear 1. Arrange the halides in order...
8. Rank these compounds in decreasing order of their reactivity in SN 1 reactions. (8 points)
1. Draw the line structures and arrange the following substrates in order of increasing SN2 reactivity with NaCN: Bromoethane, 1-chloro-3,3-dimethylpentane, 1-chloro-2,2-dimethylpentane, and 2-bromo-2- methylpentane. (1 pt) 2. Design a synthetic route for the following conversion of methylcylohexane into compound A using retrosynthesis analysis. You may use any other reagents that you need. (1 pt) 3. Predict which of the following two compounds will undergo an E2 reaction more rapidly in presence of EtONa/EtOH. Draw the reaction product(s) and the mechanism...
1. arrange Alkyl chlorides in theoretical order of reactivity in SN1 reaction 2. arrange Alkyl chlorides in theoretical order of reactivity in SN2 reaction a HC 1-Chlorobutane AgNO3+ Ethanol (SN1) Nal + Acetone SN2 CH3 H3C 2-Chlorobutane Br CH3 H3C 2-Bromobutane CH3 H2C- a CH3 t-butylchloride Benzylchloride Br Bromobenzene
1. arrange Alkyl bromides in theoretical order of reactivity in SN1 reaction 2. arrange Alkyl bromides in theoretical order of reactivity in SN2 reaction AgNO3+ Ethanol Yal H₂C (SN 1) 1-Chlorobutane Nal + Acetone SN2 CH3 H3C 2-Chlorobutane Br CH3 H3C 2-Bromobutane CH3 H2C- a CH3 t-butylchloride Benzylchloride Br Bromobenzene
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...