7. All of the following compounds that are at the same oxidation levelare ___.u. methyl epoxide, v. propyne, w. propanal, x. propene,y. 2,2-dihydroxypropane, z. isopropanol?A. u,v,w,y; B. u,v,w; C. v,w,y,z; D. v, z; E. x,y,z Please include all steps. Thank you!
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7. All of the following compounds that are at the same oxidation level
are ___.
u. methyl epoxide, v. propyne, w. propanal, x. propene,
y. 2,2-dihydroxypropane, z. isopropanol?
A. u,v,w,y; B. u,v,w; C. v,w,y,z; D. v, z; E. x,y,z
Please include all steps. Thank you!
Step by step
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- 2 3 5 [Review Topics] Reagents HBr a. b. C. H₂O, H₂SO4 d. Br₂ Cl₂ H₂, Pd Br₂, H₂O Cl₂, H₂O OsO4 then NaHSO3 e. f. g. h. i. j. k. I. [References] HBr, H₂O2, hv Hg(OAc)2, H₂O then NaBH4 BH3 then H₂O2, NaOH O3 then (CH3)2S m. n. O. p. q. r. S. t. u. V. 2 equivalents of NaNH₂ H₂, Lindlar's catalyst Na/NH3 H₂SO4, HgSO4 (sia)2BH then H₂O₂, NaOH 1 equivalent of NaNH2 NBS, hv Br₂, hv Cl₂, hv HCI Identify the reagents necessary to accomplish the following steps in the above synthesis of 3-hexanone from acetylene: Step 4: v Step 5: F Step 7: Previous Next Save and ExitPlease help with the attached question, thank you!Give detailed Solution with explanation needed..,,,!
- Give detailed Solution with explanation neededNoneWhat 3 steps would be required to complete the following synthesis? Step 1 = A Step 2 3D в Step 3= B. NABH4, CH;OH C. PCC, CH;Cl; А. , AICI; D. CrO3, H3O* G. HNO;, H;SO4 J. i.propanal, ii. H+, H;0 K. NACN, DMSO M. Žn(Hg), HCI E. TSCI, pyridine H. CH;OH, H F. Bry, Light I. Brz, FeBr; L. i.butanal, ii. H+, H2O O. another reagent N. Mg. Et,0
- Give detailed Solution with explanation needed..don't give Handwritten answer..give the product of the given reactionMATCHa structuceor.term.from the tollowing list.with.each description belom Plas the structure.or.term.inthe blank to.the Jeft.of.the description a. F-TEDA-BF b. NO d. electron-donating E. electron-withdrawing The reactive electrophile in Friedel-Crafts acylation reactions 28, The electrophile in aromatic nitration 29.- bstitution. Groups which activate aromatic rings towards electrophilic su 30 Source of F* in fluorination reactions. 31.A. Mel B B. Na, NH3 (1) C. Br2, hv Transformation A: A D L D. NaNH2 E. H₂, Lindlar's cat. F. H₂, Pt G. HBr (1 equiv.) H. 1) xs NaNH2; 2) H,O I. 1) RCO3H; 2) H3O+ Transformation B:
- Handwriting not allow pleaseAny special precautions or purifications of the reagents required? Limiting and excess reagent? Why is excess necessary? 4,4'-DIBROMOBIPHENYL [Biphenyl, 4,4'-dibromo-] Submitted by Robert E. Buckles and Norris G. Wheeler1. Checked by R. S. Schreiber, Wm. Bradley Reid, Jr., and Robert W. Jackson. 1. Procedure In a 15-cm. evaporating dish is placed 15.4 g. (0.10 mole) of finely powdered biphenyl (Note 1). The dish is set on a porcelain rack in a 30-cm. desiccator with a 10-cm. evaporating dish under the rack containing 39 g. (12 ml., 0.24 mole) of bromine. The desiccator is closed, but a very small opening is provided for the escape of hydrogen bromide (Note 2). The biphenyl is left in contact with the bromine vapor for 8 hours (or overnight). The orange solid is then removed from the desiccator and allowed to stand in the air under a hood for at least 4 hours (Note 3). At this point, the product weighs about 30 g. and has a melting point in the neighborhood of 152°. The crude…e. f. g. d. 5. Provide the structure for the major product in the following reactions. or a. b. OH 6 6 3 6 Br 1. SOCI₂, pyr. 2. 2. 2 t 1. LiAlH4 (xs) 2. H₂O 1. LIAI(OR) 3H 2. H₂O Et₂CuLi NH₂ 1. EtMgBr (xs) 2. H₂O 1. Mg 2. CO2 3. H* 4. SOCI₂, pyr 1. [H], NaBH3CN, EtNH2 O CI pyridine