Draw the cis form of the only compound that has stereochemistry: CH3 CH3 CH3 Draw the trans form of the only compound that has stereochemistry: Edit ·||||CH 3 Edit Your answer is partially correct. Try again. Name the molecule whose longest chain has five carbons: (Do not add any spaces between any terms) cyclopentane Name the molecule whose longest chain has four carbons: (Do not add any spaces between any terms) methylcyclobutane Name the molecule which has a two-carbon long chain substituent: (Do not add any spaces between any terms) Tethylcyclopropane Name the molecule that has a quaternary carbon: (Do not add any spaces between any terms) 1,1-dimethylcyclopropan x Name the form (cis or trans) of the only compound with stereochemistry: (Do not add any spaces between any terms (1R, 2S)-1,2-dimethylcyc

Draw the cis form of the only compound that has stereochemistry: CH3 CH3 CH3 Draw the trans form of the only compound that has stereochemistry: Edit ·||||CH 3 Edit Your answer is partially correct. Try again. Name the molecule whose longest chain has five carbons: (Do not add any spaces between any terms) cyclopentane Name the molecule whose longest chain has four carbons: (Do not add any spaces between any terms) methylcyclobutane Name the molecule which has a two-carbon long chain substituent: (Do not add any spaces between any terms) Tethylcyclopropane Name the molecule that has a quaternary carbon: (Do not add any spaces between any terms) 1,1-dimethylcyclopropan x Name the form (cis or trans) of the only compound with stereochemistry: (Do not add any spaces between any terms (1R, 2S)-1,2-dimethylcyc

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter6: Alkanes & Alkenes

Section: Chapter Questions

Problem 21E

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Consider rotation about the indicated bond in the molecule below. Which Newman Projection formula best represents the most stable conformer of the molecule with respect to rotation about the indicated bond? [As noted below: there is no steric strain between -H and -Et that have a gauche, staggered relationship] H CH3 Br-C-C-CH₂CH3 H. H Br CH₂CH₂ 1 CH3 H CH3CH₂ H Br H₂C || H H₂C H Br H ||| Select one: OA. I O B. II O C. III O D. All conformers have identical energies. CH₂CH3 H NOTE CH3CH₂ H no steric strain
a) Draw all Newman projections of your molecule's conformations in which the CH3 group and the H of the CHY2 group are positioned 'ANTI' to each other. Be sure to put in the correct X and Y atoms, bonded to the correct C atoms, for your molecule. X = FY=I Conformations = 60 deg and - 180 deg 60 deg dihedral angle = - 179.987 deg 180 deg · - dihedral angle = 179.814 deg
Click on all of the atoms that make up the largest coplanar unit in the molecule below. XX H H -H
3. Draw the dash-wedge structure for the following molecules. 1 C₂H₂ C₂H₂ S H CH₂ 1 H Br H Cl * H H 4. Arrange the structures in the increasing order of stability CH₂ C₂H₂ C₂M₂ C₂H₂ H C₂H₂ *馬來西 H C₂H₂ H C₂H₂ CHy CH₂ IV || |||
Draw the structure(s) of all of the possible monochloro derivatives of 2,2-dimethylpropane, C3H11CI. • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right co Separate structures with + signs from the drop-down menu. opy aste ChemDoodle >
Here is the chemical structure of 2-bromobutane: H H. H C-C-H H :Br: H H 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 relationship to 2-bromobutane CH, (Choose one) H,c=ċ=CH,-Br Explanation Check O 2021 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Center I Accessibility P Type here to search 76°F DELL F1 F2 F3 F4 F5 FB F9 F10 F11 F12 PrtScr PAA @ %23 2$ 1 8. 9 Q W R Y. A F G H. K V N4 Alt Ctri Alt Σ B. C1
Using your model, construct an energy diagram to show the variation in the free energy of the molecule as the FRONT ATOM is rotated CLOCKWISE from 0º to 360º in 60º increments. In your energy diagram, you should clearly show the relative energies of each conformer.
Assign absolute configurations as R or S to each of the following compounds. CH3 к) н COOH Br .......... CH3 NH2 L) CN M) C CH3 CH;CH CH,OH CHO N) HuC. CH2OH U... I
Choose the factor that explains this observation. || A) resonance stabilization B) charge C) electronegativity D) polarizability OH OH₂
Choose the correct answer. Choose.. Choose... An alkyne with molecular formula C5H10 A ketone with molecular formula C4H8O A ketone with molecular formula C3H8O An alkene with molecular formula C5H8 An alkene with molecular formula C5H10 An aldehyde with molecular formula C2H40 An aldehyde with molecular formula CH4O H. A saturated hydrocarbon with molecular formula C6H14 Choose..
For each organic compound in the table below, enter the locant of the highlighted side chain. CH3 CH₂ CH₂ H CH3 · C CH₂- CH CH3 CH₂ CH3- compound CH₂ I CH₂- CH CH | CH₂ CH3- — - CH₂ | CH₂-C. CH3 | — ぎーぎ CH3 locant of highlighted side chain 0 0
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