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Equatorial 3-methyl methylenecyclohexane (2) is favored over the axial isomer 1 by 1.4 kcal/mol (experimentally measured value). The 1,3-diaxial interaction energy between H and a lone pair is negligible (~ 0 kcal/mol). What is the 1,3-diaxial interaction (in kcal/mol) between a CH3 and a p orbital?
If you dissolved 0.95g of salt in 100ml distilled water, what is the concentration of salt in this solution in g/ml
A green leaf has a surface area of 2.10 cm^2. If solar radiation is 1150 W/m^2, how many photons strike the leaf every second? Assume three significant figures and an average wavelength of 504 nm for solar radiation.
You have given some aqueous solutions as a. LiClO4 b. HClO c. CH2CH3OH d. HClO4 e. HNO3 you just need to Classify each of the given aqueous solutions as a weak electrolyte, non electrolyte, or strong electrolyte ?
During the electrolysis of an aqueous solution of CuSo4 using inert electrodes, the mass of the anode remains the same but the cathode gains mass
what is the root-mean-square molecular speed of a gas molecule of this smelly gas molecule at 25C?
We place 1.32 mol PCl5 in a 1.0 L flask and allow it to reach equilibrium at a given temperature. What is the final concentration of Cl2 in the flask?
Health Canada recommends a an upper level intake of Na to be 2300 mg. How many ounces (oz) of the meat must be ingested for a person to meet this level?
A standard NaOH solution is contaminated with Na2CO3. In the titration of 50.00 mL of .1002 M HCl solution, 32.00 and 32.50 mL of base are required to reach the methyl orange and Phenolpthalein end points,
What combustion products are produced when materials made from polyacrylonitrile smolder and burn?
The molecular shape of [TeF3 ]-1 is: A. tetrahedral B. square planar C. square pyramidal D. trigonal bipyramidal E.octahedral F. T-shaped G. see-saw, butterfly, or unsymmetrical tetrahedron
Balancing the following reaction in basic solution and also Identifying the reducing and oxidizing agent. Please explain how the answers were obtained.
What reagent could be used to reduce both the nitro and ketone functional groups in a single reaction?
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