Benzene-toluene equilibrium is often approximated as αBT = 2.34. Generate the y-x diagram for this relative volatility. Also, generate the equilibrium data using Raoult’s law, and compare your results to these. post excel spreadsheet w values used to generate both graphs
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Benzene-toluene equilibrium is often approximated as αBT = 2.34. Generate the y-x diagram for this relative volatility. Also, generate the equilibrium data using Raoult’s law, and compare your results to these.
post excel spreadsheet w values used to generate both graphs
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- Construct the expression for Kc for the following reaction. CH₂(g) + 2 H₂S(g) = CS₂(g) + 4 H₂(g) Drag the tiles into the numerator or denominator to form the expression. Each reaction participant must be represented by one tile. Do not combine terms. [CH] [H₂S]² 2[H₂] 2[CH] [H₂S]* 4[H₂] Kc = 4[CH] [CS₂] [H₂)² [CH₂]² 1 2[CS₂] [H₂]* [CH]* 4[CS₂] [H₂S] [CS₂]² 2[H₂S] [CS₂]¹ RESET 4[H₂S] [H₂]Kk.52.11-8. Write the chemical reactions whose equilibrium con- stants are K1 and Kp2 for the amino acid serine and find their numerical values.
- dont provide handwriting solution...Consider the following reactions. 2CH4 (g) ⇌ C2H6 (g) + H2 (g) Kc = 9.5x10–13 CH4 (g) + H2O (g) ⇌ CH3OH (g) + H2 (g) Kc = 2.8x10–21 Calculate the equilibrium constant, Kc value for the following reaction. 2CH3OH (g) + H2 (g) ⇌ C2H6(g) + 2H2O (g)Iron(III) Chloride Test Saved BIIIU X2 | X² | → Ix Normal Alcohol FeCl3 test color Ethanol 2-Propanol 2-Methyl-2-propanol Cyclohexanol Phenol N/A Unknown ll !!
- Can yopu help me correcting this: NOTE:(I really did want you to state what IMFs exist between the acetic acid and water, and what happens to the number of them as the acid hydrocarbon chain grows, and that effect on solubility.)Why does the dehydration of an alcohol more often use concentrated sulfuric acid, H2SO4H2SO4, as the acid catalyst rather than dilute hydrochloric acid, HCl? Select one or more: Hydrochloric acid is too small to effectively react with the alcohol in the reaction. The additional water solvent from a dilute solution could reverse the dehydration reaction. Only acids with more than one proton can complete the dehydration reaction. The presence of the chloride ion could result in a competing substitution reaction.Can you please fill the rest of this chart
- Predict what will be observed in each experiment below. experiment predicted observation(choose one) Rock candy is formed when excess sugar is dissolved in hot water followed by crystallization. A student wants to make two batches of rock candy. He finds an unopened box of "cane sugar" in the pantry. He starts preparing batch A by dissolving sugar in 500mL of hot water ( 70°C ). He keeps adding sugar until no more sugar dissolves in the hot water. He cools the solution to room temperature. He prepares batch B by dissolving sugar in 500mL of water at room temperature until no more sugar is dissolved. He lets the solution sit at room temperature. It is likely that more rock candy will be formed in batch A. It is likely that less rock candy will be formed in batch A. It is likely that no rock candy will be formed in either batch. I need more information to predict which batch is more likely to form rock candy. A pair of…Ascorbic acid, H2C6H6O6, is a diprotic acid usually known as vitamin C. For this acid, pKa1 is 4.10 and pKa2 is 11.79. When 125 mL of a solution of ascorbic acid was evaporated to dryness, the residue of pure ascorbic acid had a mass of 3.64 g. Your answer is correct. Calculate the molar concentration of ascorbic acid in the solution before it was evaporated. 0.164 Hint Your answer is partially correct. What was the pH of the ascorbic acid solution before it was evaporated? pH = 2.44 What was the concentration of the ascorbate ion, C6H6062, before the solution was evaporated? i M MQuestion Type: Application. This question is related to material presented in Board 36.6. The structure of three different molecules is shown below. Note that each has a common "benzene" ring of six carbon atoms, but each has a different number of substituent OH (alcohol) groups, ranging from 0 to 2. H H || C H | с 1 H benzene H H H H C || C H I C= 1 H benzenol H H H Second most soluble in water: [Select] H || H 1 H catechol Least soluble in water (most hydrophobic): [Select ] H Rank these three molecules in terms of their relative solubility in water based on their respective chemical structures. Most soluble in water (most hydrophilic): [Select] H