Convert each representation to a Newman projection around the indicated bond. CH3 CI a. H17 CH3 Br H b. C. CH3CH2 H CH3 CH3 Br H 4 CH3 H CH3 H CH3 d. CH3 Br
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- Convert each structure to a Newman projection around the indicated bond. CH3 H CI CI H a. BrC. CI b. Br CH3 BrPossible Newman projection for following?Br H H H3C CH3 3. Draw the corresponding dash-wedge structure for each of the following Newman projections. H3C H OCH2CH3 H. CH2CH3 H H3C H H3C CH3 H H (CH3)3C H H H CH2CH2CH3 CH3
- 4. Circle any n-conjugated portions in the molecules below. Draw all resonance structures for each conjugated molecule. OCH3 H2C=CH-C=N CH3 CH2 H2Ca. H H 2. Draw perspective projection of the following newman projection or vice versa. CH₂CH₂CH₂ H Br CH3 3 H₂C-CH₂ / H₂C-CH₂ along C2-C3 as labeled CH3Hi! Can someone help me with this question? I am stuck between answer choices, thanks so much!
- . Consider the hash/wedge structure below. a. Draw the Newman projection of the bond indicated, keeping the conformation the same. НО b. Draw the Newman projection for the most stable conformation CI c. In the Newman projection for part b, label all gauche interactions.4. Draw a Newman projection of the following compound that centers along the marked bond. This one! CH3 CH3 + + HWhat is an acceptable Newman projection for the molecule shown below, looking down the indicated bond? O A. O B. H. H
- draw newman projection for the indicated bond. put largest groups anti to each other.Translate the given conformer from the wedge-and-dash drawing into its Newman projection. You might find it helpful to make a model, then manipulate it to the desired viewpoint. H3C H. Clil. Br CH3 Which Newman structure matches the conformer?Pl