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 moleculesWhich 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 isomers4
- Provide the IUPAC name for each one5. 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?
- Which of the molecules listed could be represented by the following newman projection: 'F H Select one: F O a. F O b. F-F F Ос. .F O d. FO Lov -Ō Na H₂C- H3 C H3C i_._ H3C-(H₂C)4 -CH3 + H₂C H₂O + H₂O O—(CH2)—CH + HO O= -OH (CH2),—CH3+ HỌ + HO-(CH2)4-CH3 HTDraw an expanded structural formula of pent-1-en-3-yne/ CH3-CC-CH=CH2 and then label each carbon. Indicate the longest and shortest C-H bond and predict the C—C single bond that has the highest BDE(bond dissociation energy).