Hello, can you help me to solve this and explain me how does pople nomenclature works in NMR? thanks H***HНH₂C HH3C HH₁CCIH3CRН"HHH3CH3CH&C-C-S-HH3CH3CBrHO₂NH3C-H-CH3H3C-CI--HHΟΝH3C-H*HR-CH₂H3CD₂NCOODH2CDOOC-CODHOHCHH₂C COODH

Answered: Image /qna-images/answer/012378a3-868a-4420-8bfe-c5086e418765.jpg

Answered: H *** H Н H₂C H H3C H H₁CCI H3C R Н "H…

Introductory Chemistry: A Foundation

9th Edition

ISBN:9781337399425

Author:Steven S. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Donald J. DeCoste

Chapter10: Energy

Section: Chapter Questions

Problem 21QAP

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For each organic compound in the table below, name the highlighted side chain. Note for advanced students: don't include the locant of the side chain. compound H-C=0 name of highlighted side chain - - CH₂ — CH₂ — CH₂ — CH₂ — CH₂— CH₂· - CH G H C 0 H C 0 CH3 CH - CH2-CH₂ CH2 | H C 0 CH₂ CH₂2 I CH₂ CH₂ O HOC CH - CH2CH2 CH₂ — CH₂ CH=CH2 ☑ ☐
Name ti.. organic compounds: structure name Он H H H Н— С — С — С — С — н | | || | н нн н CH, — сн,-сH, — С -ОН | н н H - C- C = 0 CH3 -
"Carboxylic acid Derivatives: Acyl Halides and Anhydrides, Esters, Amides" from your, textbook, and you will analyze presented organic compounds to find and discuss the differences between them and finally recognize what type of carboxylic acid derivative are they?
:O: || H 4 'N• Ⓒ:O z: |||| :O I H อะเว: :CI:0 Q I I I I
O O O O F F H-C-C-C-H CI CI FL LL F CI F F F C=C XE F CI F C=C1C-F
See image below
correet 1UPAC hame! SH
For eac te, click the button under the better solvent. solute Which is the better solvent? H,0 olo :0: || :0: Ar NH,- NH2 || CH3-S. - CH3 H CH3(CH,),CH3 H H || H,0 H H. H :0:
MeO,C=-co02Me (ехсess) A
CI ..*|||| Me CI Br H Br NaOH Acetone CH₂S: DMSO DMF MeOH ONa
a) b) c) d) + + CH₂CHCH3 CI OH CH₂CCI !! COOH HNO3 H₂SO4 H₂SO4 Δ AICI, AIC13
One of the first drugs to be approved for use in treatment of acquired immune deficiency syndrome (AIDS) was azidothymidine (AZT). CH3 C6 || Cs- H. N5 C8- H H. H-O- H C4 H C2-C3 H N1 N3

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H *** H Н H₂C H H3C H H₁CCI H3C R Н "H H H3C H3C H&C-C-S-H H3C H3C Br H O₂N H3C- H -CH3 H3C- CI- -H H ΟΝ H3C- H * H R-CH₂ H3C D₂N COOD H2C DOOC-COD H OHC H H₂C COOD H