Consider the following reaction: CI Mе. Он Cl-CI HCI Me Me Me A в Write a...
3. Provide the missing reagents for each transformation below. H2N сно A В Me Me сно H2N 4. Provide a detailed mechanism for each part of the Hell-Volhard-Zelinsky Reaction below. Note that this reaction is covered in our textb0ok (among many sections) and that the reaction conditions are modified slightly. Be sure to account for this and be as detailed in every step as possible. Do not create reagents that are not made logically in the pathway (no HBr essentially...
Determine the product of the following reaction. HCI ? ОН -CI ОН CI С- ОН None of these products will be formed. Coon
Provide a full mechanism for the following reaction. Include intermediates, formal charges, and curved arrows to show electron flow. Provide a full mechanism for the following reaction. Include intermediates, formal charges, and curved arrows to show electron flow. H20, H о нон, он вме OH HN
5. [5 pts] Use curved-arrow notation to write out a detailed, step-wise mechanism for the reaction listed below. Be sure to (a) include all of your lone pairs, (b) include all formal charges, (c) draw your arrows neatly and precisely, and (d) enclose intermediates within square brackets. If you get stuck, number the atoms of your reactant and the corresponding atoms in your product to help recognize what bonds are made and broken! HBr r Mechanism: +4 +
7. Provide a detailed me rovide a detailed mechanism for the following transformation. Be sure to use curved arrows, Show all relevant lone pairs and bonds, formal charges and all intermediates. Be sure to account for the appropriate stereochemistry. (5 points) NaH (1 equiv), THF Me Me
10. Provide a detailed mechanism for the following transformation. Be sure to use curved arrows, correct reaction arrows, Show all relevant lone pairs and bonds, formal charges and all intermediates. Think about what your components are and what would happen first. (5 points) HBr Me on me mé Br + Ho Me
answer all. thank you! Determine the product of the following reaction. HCI ? ОН CI ОН CI С СЕ О ОН CI None of these products will be formed. СІ ممر ОН Predict the product of the following intramolecular Aldol reaction. NaOH, HAO A i H H o Predict the product of the following reaction. H NOH H NO ONH2 НО. 'N НО. NHOH O HOH HOONH2
4. Draw a mechanism that explains the following reaction. Use the curved arrow convention and show all lone pairs and formal charges. NaOH NaCl HO1 DMF
4. Provide a detailed mechanism for each part of the Hell-Volhard-Zelinsky Reaction below. Note that this reaction is covered in our textbook (among many sections) and that the reaction conditions are modified slightly. Be sure to account for this and be as detailed in every step as possible. Do not create reagents that are not made logically in the pathway (no HBr essentially so it's a "neutral" pathway). Include all curved arrows, reaction arrows, reaction intermediates, formal charges, and any...
9. a) Write the detailed Sn1 mechanism for the reaction of (S)-3-bromo-3-methylhexane with H20, showing curved arrows, relevant lone pairs, formal charges, stereochemistry for each step. Include any transition states and/or intermediates, and name the product(s). b) A racemic mixture results from a reaction of the chiral alkylbromide starting material below, and acetate. at hope ܬ Write the complete mechanism for the synthesis. Show the curly arrows, relevant lone pairs and all formal charges for each step. Include any transition...