Complete the step-by-step mechanism, including all resonance structures, for the following reaction. Show proper arrows and...
write the full step wise mechanism for the reaction with proper charges, arrows and resonance structures and identify the major and minor structures for it. HBr Excess Her
complete the mechanism by drawing proper arrows and show all lone pairs in the reactants and products H3C + ONO CH3 сн. н. HC-a. sº H3CCI + O=s=0
Write the complete step-wise arrow.pushing mechanism for reaction shown below. Show electron flow with arrows, and be sure to include all intermediate structures. You must be very detailed in your mechanism for full credit. H2SO4
Please show the mechanism with acid. 2. Write the complete reaction mechanism for the KCN-catalyzed reaction. Show all electron flow with arrows and show all intermediate structures он CH-COOH O но CN = C H20* Who. HHCEN NAOH HO cyanolydrin + NaCN + H2O
5. Mechanism: (20 pts) Show the detailed reaction mechanism including all relevant arrows, intermediates, inorganic products, relevant resonance structures, and stereochemistry for the following reaction heat OH H-Br Step 1 step 2 Step 3 Step 4 Product(s) a. This is a Sx2/S1/E/Ez/ reduction / oxidation mechanism. b. What is the product if the starting alcohol is reacted with PBry? Product(s) with PBry c. Reaction with PBr; is a S2/S1/E/Ez/reduction / oxidation mechanism.
5. Mechanism: (20 pts) Show the detailed reaction mechanism including all relevant arrows, intermediates, inorganic products, relevant resonance structures, and stereochemistry for the following reaction. heat OH H-Br step 1 step 2 step 3 step 4 Product(s) a. This is a S2/Sx1/E/E2/ reduction / oxidation mechanism. b. What is the product if the starting alcohol is reacted with PBrz? Product(s) with PBrz c. Reaction with PBr3 is a S2/S1/Ej / E2 / reduction / oxidation mechanism.
9. Provide a proper electron-pushing mechanism (including resonance structures) using curved arrows that describes the monochlorination of p-methyltoluene. (10 pts.) CI-CI + HCI hv p-methyltoluene ci
Write the complete stepwise mechanism for the following reaction Show all intermediate structures and all electron flow with arrows. Draw the mechanism for the following reaction. Show stereochemistry for every step of the reaction.
Write the complete step-wise arrow-pushing mechanism for reaction shown below. Show electron flow with arrows, and be sure to include all intermediate structures. You must be very detailed in your mechanism for full credit. HO -CH₂CH₃ CH2CH3 -CH2CH3 CH2CH3 H2SO4
help Thank you 4. (10 pts) Draw all possible products for the following reaction including stereoisomers. Note that the addition occurs through a "syn" mechanism. Is the product solution optically active (yes or no)? 1. BAHATHF 2. NaOH, HO (8 pts) Provide a complete mechanism for the reaction below and include lone-pairs of electrons and formal charges. Show all products formed including stereoisomers. Is the product solution optically active (yes or no)? Bras 11. (8 pts) Draw all four regiochemical...