Question 6 What is the mechanism of the following reaction? o NH H30+ O Electrophilic addition...
HEN + H₂O 1 гсны CH HO NaOH Ph afra 2. a = Electrophilic addition d = Sy2 Nucleophilic substitution b = E2 Elimination e-Electrophilic aromatic substitution c=S91 Nucleophilic substitution 1= Carbonyl nucleophilic addn g=Nucleophilic subs at carbonyl(acyl Xfer) h - Conjugate (nucleophilie) addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters at for your answers 1
Na 1. Br CH2-Ph 2. Ph 6M HC OH он NH CI NHy CI NH d -Sy2 Nucleophilic substitution Nucleophilic subs at carbonyl(acyl Xfer) a Electrophilic addition b- E2 Elimination e-Syl Nucleophilic substitution e Electrophilic aromatic substitution h Conjugate (nucleophilic) addn r-Carbonyl nucleophilie 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. 2. Submit Answer Ratry Entiro Group 0 1. Cl 0 OMe...
O H2N-OH 2. нса a Electrophilic addition b-E2 Elimination d- Sy2 Nucleophilic substitution-Nucleophilic subs at carbonyl(acyl Xfer) e-Electrophilic aromatic substitution h -Conjugate (nucleophilic) addn SNI Nucleophilic substitution r-Carbonyl 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. 2. Submit Answor Retry Entire Group 9 more group attempts remaining
3. Which of the following best describes the general reaction type exemplified by peptide bond formation? O Electrophilic aromatic substitution O Nucleophilic addition O Proton transfer (Brønsted acid-base reaction) O Nucleophilic acyl substitution O Electrophilic addition
The mechanism by which acylation of an amine with an acid chloride takes place is: a) electrophilic addition b) nucleophilic aromatic substitution c) nucleophilic addition d) nuceophilic acyl substitution
он Biosynthesis of adreneline (epinephrine) он a Electrophilic addition b E2 Elimination CSN1 Nucleophilic substitution d-SN2 Nucleophilic substitution e- Electrophilic aromatic substitution r-carbonyl nucleophilic addn g-Nucleophilic subs at carbonyl(acyl Xfer) h - Conjugate (nucleophilic) addn
1. Draw an electrophilic addition that illustrates 1,2-versus 1,4-addition. Using this reaction, explain Kinetic versus Thermodynamic products. 2. Explain resonance hybrid and draw an example that has at least 3 reasonance forms. 3. Draw a typical Diel-Alder reaction. Show the mechanism for your reaction 4. Use the inscribed polygon techiques to illustrate why benzene is aromatic and cyclopentadiene is not 5. Draw the general mechanism for electrophilic aromatic substitution 6. Explain how substituents on the aromatic ring activate or slow...
CO2H CO2H HNO3/H2SO4 H20 2. +conc. HBr H20 Br OH a Electrophilic addition b E2 Elimination c-SNI Nucleophilic substitution d S2 Nucleophilic substitution e-Electrophilic aromatic substitution f-carbonyl nucleophilic addn g = Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn for your answers 1. 2.
T o mateh Dashboard | Resum... Module Library In... th th CASA In Link EXCESS NH Ethanol • на g - Nucleophilic subs at carbonyla h - Conjugate (nucleophilic) addin d - Sy2 Nucleophilic substitution Electrophilic aromatic substitution f-Carbonyl nucleophilic addn a - Electrophilic addition b-E2 Elimination C-S1 Nucleophilic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -i for your an 2. 2 more group attempts remaining...
This reaction, which is typical of carboxylic acids and their derivatives, is called wo- OH OH O A Nucleophilic acyl addition. O B Nucleophilic non-acyl substitution. O C Electrophilic acyl addition. O D Nucleophilic acyl substitution. O E Electrophilic acyl substitution.