Determine the systematic (IUPAC) name for each of the molecules represented by the Newman projections below. Newman Projection IUPAC Name H₂C Br. H -CH3 ☐ H CH3 H. CH3 $ H H H CI H CH3 Br CI HA -H ☐ 0
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- I dont know how to find the IUPAC name for these two moleculesPlease don't provide handwriting solutionWhich of the following molecules are isomers? (Make sure you can see all of all three structures.) ннн нннн H нн ннн H-C-C-Ċ-Ċ-OH H-C-0-Ċ-Ċ-Ċ-H H-C-C-0-C-C-C-H нннн H ннн нн ннн I II III O , I, and II O I and II I and III Il and III None of the molecules are isomers
- Br Hu Br 7 CI ECH H,C=CH 4 HC=CH HC=C Br HC=CH H2C=CH2 1Provide the IUPAC name for each oneO B) II O A) I O D) IV OC) III Question 17 O FLY Which of the following is the correct Newman projection for the following compound as viewed down the indicated bond in the conform CI. H Br CH3 H Br CH3 1 CH3 H CH3 11 H Br CH3 H ||| CH3 Br Η. Bri CH3 CI IV CH3 H CI Br CH3 H H CH3 V
- 4. Designate R or S of the followings. Br C3H7 COOH C-H b) HS H CC2H5 с) Hас— он a) H a CHO a CH3 H. g) HO ČH3 e) OH f) b. H- -CI Br- -H :) ČH3 H- -CI OH5. a-G a- Convert the following Newman projection into the bond line structural formula. Must use stereobonds to indicate the orientation of the groups. H3CO CN b- Draw the anti, gauche, and eclipsed conformations of the following molecule using Newman projection. H H H H c- i. Which cyclopropane molecule has the highest torsional strain? ii. Which cyclopropane molecule has the lowest torsional strain? C b aExplain why these two molecules are not isomers:
- Here is the chemical structure of 2-bromobutane: Н Η Н Н HHHH C C- C C-H H :Br Η Н .. Decide whether each molecule in the table below is another molecule of 2-bromobutane, a molecule of an isomer of 2-bromobutane, or a molecule of an entirely different compound. molecule CH₂ CH₂-CH₂-CH-Br CH₂ CH₂ -CH₂ Br HI H H H Η H_ H-C- C-C- H-C-H H H relationship to 2-bromobutane (Choose one) (Choose one) Br: a molecule of an isomer of 2-bromobutane ▼NiteshWhat are the IUPAC names?