For each reacttion below suggest stuctrues for alkenes that give the indicated reaction products.
The information given for this problem is 1.BH3,THF / 2. H2O2,NaOH, H2O Those are the catalyst and the major product for this question is 3-methyl-2-pentanol. I need to find the base for this mechanism.
For each reacttion below suggest stuctrues for alkenes that give the indicated reaction products. The information...
Predict the products the alkenes shown below would produce on exposure to each of the reagents (i)-(iv) (4 reactions X 5 alkenes = 20 products). Pay attention to both regiochemistry and stereochemistry (syn or anti addition). You may draw just one enantiomer of any chiral product, though both enantiomers will be produced in equal amounts. (i) BH3, then NaOH, H2O2 (ii) Hg(OAc)2 in H2O, then NaBH, (iii) Bra in CH3CH2OH Autumn 2019 EM 223 (iv) Cl2 QUÝ" H H
In each reaction box, place the best reagent and conditions from the list below. CH3 2) 3) H2, Lindlar catalyst H2O, H2SO4 CH3CH2Br Br2 bromocyclohexane BH3/THF SOCl2 excess NaNH2 HBr CH3Br H2O2, NaOH, H2O
2. Draw the major product(s) from the reaction of the starting material below with the following reagents: (12 marks) (a) (b) (1) BH3, THF (2) H2O2, NaOH, H2O Cl in excess EtOH (0) I-CI (d) (1) O3. CH CI: (2) Zn, acetic acid (e) (1) (1) OsO4, THF (2) H2S (1) Hg(OOCCH3)2, H2O (2) NaBH4, NaOH, H2O
Give the major organic product(s) of the reactions of l-methyl-2-deuteriocyclohexene (D = "H) with the reagents given. Be sure to show all stereoisomers formed, and indicate which isomers are formed in equal and in unequal quantities. CHE 1-methyl-2-deuteriocyclohexene (a) (1) BH, THF: (2) H:03, NaOH, H:0 (b) HBr, AIBN (c) Br, H:0 Give the major organic product(s) of the reactions shown below. Be sure to show all stereoisomers formed, and indicate which isomers are formed in equal and in unequal...
In each reaction box, place the best reagent and conditions from the list below. Please give a brief explanation for your response so I can understand it better. Thanks! In each reaction box, place the best reagent and conditions from the list below. (A reagent may be used more than once.) CH3CH2Br NaOH H2O2/NaOH H30+ CH3br NaBH4 NaNH2 CH3CH2CH2CH2Br CH3CH2CH2Br H2, Lindlar catalyst BH3/THF
I need two products and I am not sure what I am getting wrong. Problem 8.46 (c) Predict the major products of the tollowing reaction, and give the structures of any intermediates. Include stereochemistry where appropriate. CH2 (1) BH3 THF (2) H2O2, OH Draw the molecules on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars, including charges where needed. The single bond is active by default. Show the appropriate stereochemistry by choosing the...
What is the percent yield from the reaction? Show calculations, including those for the limiting reactant? Starting (reactant) is 1-methyl-1cyclohexene and the arrow says 1. BH3*THF 2. H2O2, NaOH . The product is trans-2-methylcyclohexanol. the mass of the alkene is 0.41 grams the mass of BH3*THF is 2.45 grams The mass of the product is 1.2477 grams What is the percent yield from the reaction? Show calculations, including those for the limiting reactant?
In each reaction box, place the best reagent and conditions from the list below. In each reaction box, place the best reagent and conditions from the list below. 2 equiv. NaNHz excess NaNH2 CH3Br H20, H2SO4, HgSO4 Na, NH3 (1) H2O2, NaOH, H2O NaBH4 HBr Br2 CH3CH2Br H2. Lindlar catalyst BH3/THF PBr3
1. Give the major product of the following reactions, write NR. if no reaction happens. Indicate the stereochemistry if necessary CHCI KOC(CH3). (CH),COH 1. conc. HBr, heat 2. KOBU, HOBU 1. NaOM, MOH CI 2. BICN 1. 1 eq. BH3. THE 2. H2O2, NaOH, H2O 3. Hg(OAC), MeOH 4. NaBH4, NaOH, H2O 1. conc. HCI 2. LDA, THF 3. O. CH,OH 4.(CH), 1. Hg(OAC), THE 2. NaBH, NaOH, H2O > OH (Hint: product has a bicyclic ring)
Dehydrohalogenation - 30 and 2° alkyl halides are converted to alkenes by treatment of strong base. Dehydrohalogenation occurs through a concerted reaction mechanism. КОН ethanol Major Product Mechanism Zaitsev's rule - Dehydration - 30 and 2° alcohols are converted to alkenes by treatment with an acid catalyst. Acid catalyzed dehydration. H2SO4, H,0 THF, 50°C Major Product Mechanism Cyelopropane via Carbene generation-treatment of chloroform (CHCI) with base leads (KOH) to the formation of a Dichlorocarbene: HSC C: CI-C-H + KOH HC...