The reaction is
Trans- 1,2-dibenzoyl ethylene …………………………….> Cis- 1,2-dibenzoyl ethylene
Mol. Wt. : 236.26 g/mol 236.26 g/mol
From the above transformation
236.26 g of trans-1,2-dibenzoyl ethylene produces cis-1,2-dibenzoyl ethylene = 236.26 g
0.192 g of trans-1,2-dibenzoyl ethylene produces cis-1,2-dibenzoyl ethylene = 0.192 g
Theoretical yield = 0.192 g
Actual yield = 0.082 g
% yield = (Actual yield/Theoretical yield) x 100% = 42.71%
If you began with 192 mg of trans-1,2-dibenzoylethylene and recovered 82 mg of cis-1,2-dibenzoylethylene, what is...
quesuun 14 pong If you began with 145 mg of trans-1,2-dibenzoylethylene, how much cis-1,2- dibenzoylethylene do you expect to get, if 100% of the trans was converted to the cis isomer? Aamori
In Organic lab we are enabling trans to cis isomerizaton of E-1,2-dibenzoylethylene by irradiating the alkene with UV light. What is the overall equation for this reaction? And which is more polar the trans or the cis? Why?
1) When you measured out one mL of the trans-1,2-dibenzoylethylene in ethyl acetate solution it had a mass of 0.890 grams. (0.050 g of yellow solid and rest of it is Ethyl acetate). The forerun of ethyl acetate had a mass of 0.075g and the rest of the ethyl acetate collected had a mass of 0.253 g. The trans-1,2-dibenzoylethylene had a mass of 0.046 g. What is the percent recovery of each of the materials?
Can someone explain why the answer is not cis-1,2-cyclohexanediol and ethanol? Question 7 What are the products of the reaction shown below? O CH heat O IH OA. cyclohexanone and ethanol O B. cis-1,2-cyclohexanediol and ethanol O C. trans-1,2-cyclohexanediol and ethanol O D. cyclohexanone and ethanal 0 E. cis-1,2-cyclohexanediol and ethanal
We learned that to create vicinal diols from alkenes, the cis-1,2-diol or trans-1,2 diol required very different reagents. This isn't always the case and one notable reaction that defies this convention is the Prévost reaction! (4 points) To make the cis-diol, we typically use osmium tetroxide (catalytic amounts!). What other reagent combination would work for this particular transformation? a. OH OH (rac b. (4 points) To make the trans-diol, what reagent combination would be employed? ?? 1F2 OH (4 points)...
The cis-configuration of 2-butylene is higher in energy than the trans-configuration by 8.3E‑21J. You can synthesize trans-butylene with 100% yield. A customer wants to purchase your product but insists on 99.999% trans. What is the maximum temperature you can allow the product to be stored at to meet the customer’s specifications?
You are monitoring the decay of 13-cis-retinal to all-trans-retinal. Initially, your sample contains 100% 13-cis-retinal. After 5 minutes, you see that 55% of your sample has converted to all-trans-retinal. Assume that the all-trans-retinal cannot convert back to 13-cis-retinal. a. What is the rate constant that describes the transformation of 13-cis-retinal to all-transretinal? b. How long will it take for 95% of the sample to be converted to all-trans-retinal?
4) What term describes the structural relationship between cis-1,2-dimethylcyclopentane and trans-1,3-dimethylcyclopentane? A) not isomers B) constitutional isomers C) enantiomers D) diastereomers E) conformers 5) How many asymmetric carbons are present in the compound below? CH H (CH)CH A)0 B) 1 C) 2 D) 3 E) 4 6) What term describes the structural relationship between (2R,3R,4S)-2,3,4-trichloroheptane and (25,3S,4R)-2,3,4-trichloroheptance? A) not isomers B) constitutional isomers C) enantiomers D) diastereomers E) conformers
1. If you began with 0.5296 g of copper mesh and recovered 0.2937 elemental copper, what would be the percent recovery of copper metalo 2. Describe the differences in the appearance of the copper mesh vs. the appearance of the elemental copper at the end of the reaction sequen Why should you be careful not to overheat the crude copper metal in the evaporating dish. Which reaction do you think might occur if the sample is heated too strongly? How...
i know with E pentene it would be trans and Z pentene it would be cis. but im confused at to what that has to do with heat of hydrogenation 16. Which has the smaller heat of hydrogenation, (E)-2-pentene or (Z)-2-pentene? What is the structural origin of this difference? Please give your answer here: