1-Bromopropane is treated with each of the following reagents. Draw the major substitution product if the...
list the products of 1-bromopropane with each of the following reagents. indicate the major product. write "no reaction" where appropriate. s t the products of the reaction of 1-bromopropane with each of the following reagents indicate the major product. Write "no reaction where appropriate (a) KOH (b) Csi (e) NaSCN (h) NaNa (c) NaCN (f) CHEON (d) NH3 (g) NaSH (i) Ki
Draw the missing major organic product(s), starting material(s), or reagents for each of the following reactions (DO NOT WRITE +EN AS A PRODUCT (ie draw everything out!)! And remember stereo and regiochemistry.) Assume reagents are in excess unless otherwise indicated. **To make things simple, I indicated what is needed for each section! Please don't just put the answers, but explanations as well on why. Thanks! a) draw the starting material for this reaction. b) draw the product for this reaction....
1) Which base yields the most SN2 when treated with the same starting material? (draw this structure with stereochemistry) 2)Which base would have the least yield of SN2? 3) What conclusions are made about the amount of SN2 product formed as a function of base strength? 4) Discuss stereospecificity of an SN2 reaction and draw the SN2 transition state intermediate formed when benzoate is treated with starting material. 4. When the starting material shown below is treated with a variety...
1. (7 points) Draw the major, organic product generated for each of the reactions regiochemistry and stereochemistry. Be sure to indicate if more than one enantiomer is formed. below. Pay particular attention to the CI dilute H2SO4 KCN C2, H20 (dark) 1. BH3 THF 2. H2O2, KOH 1. NaH 2. allyl chloride (e) Draw the stereoisomer of 2,3-diphenylbut-2-ene that yields meso-2,3-dibromo-2,3-diphenylbutane on reaction with Br2 in the cold, darkness. 2.(2 points) Complete the following synthesis by filing in the missing...
For the reagents below, draw the major organic product of the bimolecular substitution and use curved-arrow notation to draw the mechanism. Be sure to draw any non-bonding electrons. For the reagents below. draw the major organic product of the bimolecular substitution and use curved arrow notation to draw the mechanism. Be to draw any non-bonding electrons. Draw curved arrow(s) Draw product DMSO Na
Draw the substitution product formed (including stereochemistry) when (R)-hexan-2-ol is treated with each series of reagents: (a) NaH, followed by CH3I; (b) TsCl and pyridine, followed by NaOCH3; (c) PBr3, followed by NaOCH3. Which two routes produce identical products?
Aromatic substitution Give the major product of the following reaction. HNO, OH HSC HC Give the major product of the following reaction: HASA Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene. Give the major product of the following reaction. Give the major product of the following reaction. Draw the starting material if no reaction occurs. Give the major product of the following reaction. Draw the starting material if no reaction occurs. NO 2 Give the major product of...
Draw the structure(s) of the major organic product(s) obtained after workup of the following reaction. NaOH O-S CH3 excess NH2 workup . You do not have to consider stereochemistry. If no reaction occurs, draw the organic starting material. Draw structure(s) of product(s) after workup to neutralize acid. Include counter-ions, e.g., Nat, I, in your submission, but draw them in their own separate sketcher. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner....
Question 4: Starting with 2-methyl-1-propanol, draw the organic product formed when treated with the following reagents: OH 2-methyl-1-propanol a) H.SO,, heat HCI c) 1) TsCl, py PBr 2) NaSH
a) Draw the major organic substitution product (ignoring stereochemistry) formed in the following reaction. b) If the reactant's configuration were (1 R,2R), then the configuration of the substitution product(s) will be (select all that apply): 1R, 2R. 1S, 2S. 1R, 2S. 1S, 2R.