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- A chemist allows some pure (2S,3R)-3-bromo-2,3-diphenylpentane to react with a solution of sodium ethoxide(NaOCH2CH3) in ethanol. The products are two alkenes: A (cis-trans mixture) and B, a single pure isomer. Under thesame conditions, the reaction of (2S,3S)-3-bromo-2,3-diphenylpentane gives two alkenes, A (cis-trans mixture) and C.Upon catalytic hydrogenation, all three of these alkenes (A, B, and C) give 2,3-diphenylpentane. Determine the structuresof A, B, and C; give equations for their formation; and explain the stereospecificity of these reactionsWhich of the following compounds will react with isopropyl magnesium bromide to give 2,4-dimethylpentan-2-ol?Name the following compounds properly, including stereochemistry. CH3 H3C a) b) он Br e leom d Son lasal Br cle e en S) Draw the structures of the following compounds. a) acetonitrile Jud iyrdem snonet b) benzonitrile c) acetic acid d) formic acid outoge e) propyl propanoate y o trans Draw specific (no R's) examples of: the tet a) a hemiacetal b) a phosphorus ylide. c) an acid chloride d) a hydrate The reaction of acetone with NABH4 is a) a hydration b) a hydrolysis c) an oxidation d) a reduction pts) "Soap" may be defined as: a) a long chain carboxylic acid b) the sodium salt of a long chain acid c) the methyl ester of a long chain acid d) an anhydride of a long chain acid
- Draw the structure of the expected organic product(s) formed in the following reactions including correct stereochemistry. If the product is racemic write racemic or draw both isomers. Assume all reagents listed are present in excess unless otherwise noted. If no reaction occurs, state "No Reaction".A chemist allows some pure (2S,3R)-3-bromo-2,3-diphenylpentane to react with a solution of sodium ethoxide(NaOCH2 CH3) in ethanol. The products are two alkenes: A (cis-trans mixture) and B, a single pure isomer. Under the same conditions, the reaction of (2S,3S)-3-bromo-2,3-diphenylpentane gives two alkenes, A (cis-trans mixture) and C. Upon catalytic hydrogenation, all three of these alkenes (A, B, and C) give 2,3-diphenylpentane. Determine the structures of A, B, and C; give equations for their formation; and explain the stereospecificity of these reactions.1) Provide the name for each structure shown. NO ₂ 2) Draw the structure of the molecule with the following name: a) (1R, 3S)-Cyclopent-4-ene-1,3-diol b) (2R, 3Z)-3-Chloro-2phenylhex-3-enal c) (2E,4Z)-Hepta-2,4,6-trienoic acid d) (3R, 4E)-3-isopropyl-6-oxohex-4-enenitrile H₂C NH CH3 CH3 H₂N CH3
- what is the structure of the substitution product in the following reaction and consider stereochemistry in deciding your product?What is (are) the major organic product(s) obtained from the following reaction? Br2 O (2R,3R)-dibromobutane meso-2,3-dibromobutane O (2S,3S)-dibromobutane O Racemic mixtureDraw the structure of the expected organic product(s) formed in the following reactions including correct stereochemistry. If the product is racemic write both isomers or write racemic. Assume all reagents listed are present in excess unless otherwise noted. If no reaction occurs, state 'No Reaction'
- Give IUPAC name for the following compounds: (Specify stereochemistry when shown in the diagram.) Ph Hi CH3CH2 1st compound: 2nd compound: H HO OH "H H CHCH₂CH₂CH318:44 1 Reset Question 4 of 12 CI Provide the correct IUPAC name for the skeletal (line-bond) structure shown here. Stereochemistry is ignored. 5Gº CI Submit 2- 1,2-3,4- 1,1- 2,2- 1- tert- di tri cyclo sec- iso meth carbo) prop bromo) chloroeth ane yl ene yne Tap here or pull up for additional resourcesDraw the structure of the expected organic product(s) formed in the following reactions including correct stereochemistry. If the product is racemic write both isomers or write racemic. Assume all reagents listed are present in excess unless otherwise noted. If no reaction occurs, state 'No Reaction'