Lets show the gauche and anti conformation.
H -bonding is present in gauche conformation and not in Anti due to the orientation of OH group. H-bond makes gauche conformation more stable.
Ethylene glycol (CH2OHCH2OH) is unusual in that the gauche conformation is more stable than the anti...
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.
Understanding Conformation Analysis Draw two Newman Projections for a n-pentane that depict and anti and gauche conformation looking down the c2-c3 bond. Which conformation is the most stable and why?
Using Newman projection draw an eclipsed, gauche, and anti conformation for the compound brlow and indicate which is the most stable. 2-Iodobutane (C2-C3 bond)
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...
The anti conformation of 1, 2-dichloroethane, Cl-CH_2-CH_2- Cl, is 4.81 kJ mol^-1 (1.15 kcal mol^-1) more stable than the gauche conformation. The two energy barriers (measured relative to the energy of the gauche conformation) for carbon-carbon bond rotation are 21.5 kJ mol^-1 (5.15 kcal mol^-1) and 38.9 kJ mol^-1(9.3 kcal mol^-1). Sketch a graph of potential energy versus dihedral angle about the carbon-carbon bond. Show the energy differences on your graph and label each minimum and maximum with the appropriate...
When water is added to ethylene glycol, the viscosity of the solution decreases when compared to pure ethylene glycol. Which of the following is the BEST explanation of why this occurs? Ethylene glycol is thick and water is thin, so when mixed together it makes a medium thick solution The water molecules increase the intermolecular interactions between the ethylene glycol molecules, which allow them interact with other molecules, the resulting solution less viscous. The water molecules increase the intermolecular interactions...
осс Стриотсуттогасити рта 9 часосото. Draw a wedge-and-dash structure of the lowest energy anti-gauche conformation of pentane. Explicitly draw out ALL hydrogen atoms on the first 4 carbons. Draw the last CH3 without explicitly drawing out its 3 hydrogen atoms. Edit
Be sure to answer all parts. Ethylene glycol (EG), CH (OH)CH (OH), is a common automobile antifreeze. It is water soluble and fairly nonvolatile (b.p. 197°C). Calculate the boiling point and freezing point of a solution containing 557.5 g of ethylene glycol in 2881 g water. The molar mass of ethylene glycol is 62.07 g/mol. Boiling point: Freezing point: I °C
Be sure to answer all parts. How many liters of the antifreeze ethylene glycol [CH2(OH)CH2(OH)] would you add to a car radiator containing 7.25 L of water if the coldest winter temperature in your area is -21.0°C? Calculate the boiling point of this water-ethylene glycol mixture. (The density of ethylene glycol is 1.11 g/mL.) What is the volume of antifreeze? L. What is the boiling point of the solution? oC
i know that trans is more stable than cis but i really confusion between 2 and 4. please give me the answer with clear explanation and clear writing. i dont know anything about bulky group 5. Which of the following is the most stable conformation of trans-1-ethyl-3-methylcyclohexane? CH.CH CH2CH3 ÇH CH3 CH3 CH2CHE CH2CHE - C O (A) 1 (B)2 O(C) 3 O (D) 4