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Give the IUPAC name for each compound. (include R,S designation or E, z configuration if needed)
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- Draw the structure of an alkyl bromide with molecular formula CgH13Br that fits each description: (a) a 1° alkyl bromide with one stereogenic center; (b) a 2° alkyl bromide with two stereogenic centers; (c) an achiral 3° alkyl bromide.(a) H3C OH (c) HBr Ether (e) CH3CH₂CHBrCH3 (f) CH3CH₂CH₂CH₂Br ? NBS hv, CCl4 Mg Ether Li Pentane (g) CH3CH₂CH₂CH₂Br + ? A? A? (CH3)2CuLi (b) CH3CH₂CH₂CH₂OH (d) H₂O CUI Ether B? B? ? OH PBr3 Ether SOCI₂ ?Give a common name (when possible) and a systematic name for each compound. ) (h) CH3C‚CCH2OCH3
- 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 CHCH₂CH₂CH3IUPAC name of the following compound is: OC-H5 OCH3 OCH3 A 1-Ethoxy-2,2-dimethylcyclohexane (B 1-Ethoxy-2,2-dimethoxycyclohexane C 2-ethoxy-1,1-dimethoxybenzene D 2-Ethoxy-1,1-dimethoxycyclohexane1. Name compounds by IUPAC nomenclature CH₂CH-COOH a ОН 2) Find all of the heterofunctional compounds among following: ОН 2 сн, -ен, -с NH, OH COOH CH-OH CH,COOH e b COOH H-C-OH н-с- -ОН COOH -СООН f с H₂C-C-CH₂ 0 COOH HO-C-CH,COOH CH,COOH CH2-CH-CH2; OH ОН ОН g d ОН HOOC–C–CH,COOH ОН HOỌC –COOH б ONa
- Write the IUPAC name of each compound, showing stereochemistry where relevant.Name of the next compound according to IUPAC rules? 10 nwn Tp ן שילה , Br of -A is buiis Jail(a) Draw all products formed by treatment of each dibromide (A and B) with one equivalent of NaNH2. (b) Label pairs of diastereomers and constitutional isomers. H Br H Br CH3 CH3 Br H H Br A
- (a) Give the IUPAC name for A and B. (b) Draw the product formed when A or B is treated with each reagent: [1] NaBH4, CH3OH; [2] CH3MgBr, then H2O; [3] Ph3P = CHOCH3; [4] CH3CH2CH2NH2, mild acid; [5] HOCH2CH2CH2OH, H+.Draw the organic products formed when cyclopentene is treated withfollowing reagent. [1] CH3CO3H; [2] H2O, HO−Chondrocole A is a marine natural product isolated from red seaweed that grows in regions of heavy surf in the Pacic Ocean. (a) Predict the solubility of chondrocole A in water and CH2Cl2. (b) Locate the stereogenic centers and label each as R or S. (c) Draw a stereoisomer and a constitutional isomer of chondrocole A.