Here you go:
The wedge-dash conformation is the one where the two hands of the carbon atom are in the plane and the rest of the two are above and below the plane accordingly and the anti-gauche confirmation is represented here for the pentane. The drawing looks like:

осс Стриотсуттогасити рта 9 часосото. Draw a wedge-and-dash structure of the lowest energy anti-gauche conformation of...
Challenge Problem 09.78 The two lowest energy conformations of pentane are the anti-anti and the anti-gauche forms, in terms of arrangements around the two central C-C bonds. A recent study analyzed the conformations of 3-heptyne as an "elongated" analogue of pentane, where a carbon-carbon triple bond is "inserted" between C2 and C3 of pentane (J. Phys. Chem. A. 2007, 111, 3513-3518). Interestingly, the researchers found that in each of the two most stable conformations of 3-heptyne, C1 and C6 are...
Gei heip answering MoTecuiar Drawing Draw a wedge-and-dash structure of the conformer of 3-heptyne that is analogous to anti-anti pentane. Explicitly draw out ALL hydrogen atoms. Edit
9.78 The two lowest energy conformations of pentane are the anti-anti and the anti-gauche forms, in terms of arrangements around the two central C─C bonds. A recent study analyzed the conformations of 3-heptyne as an “elongated” analogue of pentane, where a carbon-carbon triple bond is “inserted” between C2 and C3 of pentane.[15] Interestingly, the researchers found that in each of the two most stable conformations of 3-heptyne, C1 and C6 are nearly eclipsed (looking down the alkyne group). In one...
A) this corresponds to an anti conformation in general, gauche conformations possess the lowest post it is stabilized by intramolecular hydrogen bonding D) it is a staggered conformation. E) it has the highest energy of all the possibilities sible minimum e gy Section 2 Give the IUPAC name corresponding to the followin onding to the following structure: ection formula for the most stable conformation of the C2-C3 2) Draw the Newman projection formula for the most stable bond in 3-methylpentane.
7. Draw a wedge and dash structure of the following Newman projection GHz ви HBr CH3 t Br 8. Which of the following is a gauche conformation for butane? Which is the least stable conformation? The most stable? What is the dihedral angle for conformation ? нсна н CH... HOC CH3 сна нен нан, нен нен н" нэн IV 9. What is the IUPAC name of the following compound?
Draw the structure of the product of this reaction. Use the
wedge and dash tools to indicate stereochemistry of substituents on
ring. Do not draw hydrogen atoms. If no reaction occurs, signify
this by drawing ethane in the sketch pad.
3. Draw butane in wedge and dash depiction, sawhorse depiction and in its Newman projection looking down the 2.3 bond. Show eclipsed, gauche and anti forms. 4. Draw all Newman projections of 2-methylhexane showing eclipsed, gauche and anti forms. Rotate about the 3.4 carbon-carbon bond and watch what happens to the Draw a potential energy diagram for the rotation about the 3,4 carbon- carbon bond plotting Potential Energy versus Torsion Angle.
3. (a) A bond-line (dash/wedge) structure for butane is shown below. Using the Newman projection templates provided, draw the overall lowest energy (most stable) and overall highest energy (least stable) conformation possible in Newman projection form sighting down the bond indicated. Provide a brie explanation to justify the conformer shown for cach case. (2pts each correct Newman, 2pts for valid explanation) sight down CG- bond Lowest Energy (most stable) Highest Energy (least stable) Explain: (b) For the bond-line structure below...
Draw the most and least stable conformation of 2,4-dimethylheptane as a wedge-dash structure down the C3-C4bond (place C1 on the left). Clearly label which is the most and which is the least stable.
Draw cis-1-ethyl-3-isopropylcyclohexane in its lowest energy conformation. -draw chair conformer in lowest energy conformation -include all of the hydrogens