I know what the final product is, I need help with the reaction mechanism. Please draw and explain reaction mechanism that forms the final product.
I know what the final product is, I need help with the reaction mechanism. Please draw and explain reaction mechanism that forms the final product. M) OH 1. Na2Cr207, H2S04 N) 1. PCI 5 S ONa 2 pyridi...
REACTION IS WITH PCL3 need help with the final product and mechanism , i know you cannot gave both wedges on the same carbon so do i have to rotate it somehow on the carbon where he OH and CH3 are at ?
1. Draw the final product of the following reaction OH PBt3 2. A key precursor step in the synthesis of Albuterol involves ring opening of an epoxide 3. Draw the final product for the reaction ?? [1] NaH [2] SH 3] H20 CI 4. Draw the product for the following reaction OH CH3 POCI pyridine 5. Complete the following mechanism (the first step is shown below): Co-s-oH H3C-C-C-CH2
Please help with #3, need full mechanism, thank you! 2) Draw the major product for the base-catalyzed reaction below. OH o Na' 3) Predict the major thermodynamic product for the elimination reaction below.
9) Draw the product(s) for the following reaction. 3pts 1 eq. HNO3 H2S04 10) Select the product for the following reaction. 2pts Excess HNO3 ? H2SO4 1hr NO2 NO2 NO2 -NO2 B с D NO2 NO2 11) Provide the full mechanism for the following reaction (use as much space as you need). 5pts HNO3 NO2 H2SO4
Please explain. I need both part a and b. thank you. 2. Alcohol Reaction Mechanism Fill in the major organic product and draw a complete curved-arrow mechanism a. H-Br OH b. How would the above reaction change if sulfuric acid were used instead? Why?
Predict the product(s) for the following reaction series: 1) NaH 2) Br OH ONa O + OH
please help me 1. Provide the product/s and mechanism for the following reaction. Explain if the reaction condition favors a SN1 or SN2 mechanism. Determine the stereochemistry configuration (S/R) o the product/s. (25 points) NaCN DMSO
2. Please draw the major product(s) of the following reaction and show the mechanism. Is there a reason why one stereochemistry is preferred over the other for this reaction? points) I
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyridine Ig 1) NaH; 2) CH3CH2Br b NaH e PBr3 h 1) TSCI, pyridine; 2) NaSH c HBr f TsCl, pyridine 3. Draw the organic product formed when l-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs. a KH c HBr Te NaHCO3 b Nacid HCI f 1) KH; 2) CH3CH2Br Draw two different routes to each of...
Only need help with #5, please. 5) Draw the product(s) of the reaction of (R)-3-chloro-1-butene with BH:/HO2. Indicate stereochemistry. (20 pts) 6) What are isomers and how are they classified. (10 pts)