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Post-Lab Questions 1. (4 points) Draw the mechanism...
1. Draw the mechanism of the reaction you performed in this lab using the same starting...
1. Draw the mechanism of the reaction you performed in this lab using the same starting materials you used. You can start from the diazonium salt (you don’t need to show how the amine is converted into a diazonium). What is the name of the final product? Starting Materials used: metanilic acid (3-aminobenzenesulfonic acid) and salicylic acid
Convert playlist Diction QUESTIONS 1. (2 Points) Why is it essential to keep the diazonium salt...
Convert playlist Diction QUESTIONS 1. (2 Points) Why is it essential to keep the diazonium salt at zero degrees while you are preparing the sodium 2-naphthoxide solution? 2. (2 Points) Would you need to use sodium carbonate for the diazotization of meta- nitroaniline? Explain your answer. 3. (2 Points) What would be the IUPAC name for the azo dye if you would have used p-chloroaniline instead of sulfanilic acid? Experiment 12 4. (4 Points) Calculate the theoretical yield for Orange...
Please draw the mechanism with the compounds listed below 4 9-4: Transesterification For this assignment, the...
Please draw the mechanism with the compounds listed below 4
9-4: Transesterification For this assignment, the target compound that you should synthesize is ethyl propionate. This is a carboxylic acid derivative transformation. Keep in mind the mechanism and the potential of reaction reversibility. Examine the product and determine the bond that will be formed. Synthesis Procedures 1. Start Virtual ChemLab and select Transesterification from the list of assignments on the whiteboard. After entering the synthesis laboratory, use the available reagents...
i need all Post Lab Questions: type in your answers to the following questions Determine what...
i need all
Post Lab Questions: type in your answers to the following questions Determine what effect the following errors would have on the value for the mass percent water for your hydrate 1. The hydrate was not heated long enough to drive off all the water a. This error will increase decrease leave unchanged the mass in grams for the suminum Eproma after heating b. The error for mass of the aluminum dish Epsom salt after heating that you...
I need help with my pre and post lab questions. The three compounds below were spotted...
I need help with my pre and post lab questions.
The three compounds below were spotted on a TLC plate and developed to give the TLC plate shown. Which compound corresponds to which spot? Calculate the Rf value for spot B in the TLC plate shown above. When using polarity to determine the relative rates at which organic compounds travel up the TLC plate, we are considering compounds of similar molecular weight. It should also be noted that Rf values...
4:58 4 LTE Object POST-LAB Questions and Image Distance - Thin Lenses NAME JAIME 1. The...
4:58 4 LTE Object POST-LAB Questions and Image Distance - Thin Lenses NAME JAIME 1. The function of lenses is based on the law of refraction A light beam is traveling from the medium 1 where its speed is V., to the medium 2 where its speed is V2 = 0.8 V, a) If the first medium is the air (n = 1), what is the index of refraction for the second medium? b) If the angle of incidence is...
Please help with pre-lab questions. Pre-Lab Questions: 1. A sample of 2-butanol has a specific rotation...
Please help with pre-lab questions.
Pre-Lab Questions: 1. A sample of 2-butanol has a specific rotation of +3.25. Determine the optical purity (%ee) and percent composition of this sample (see Mohrig section 17.4). The specific rotation of pure (+)-2-butanol is +13.0°. 2. The equation for the formation of the diastereomeric salts is shown in the background information (performed in Part A of the procedure). Write this chemical equation in your notebook, then ALSO write a balanced equation for the formation...
Pre-lab Questions 1. An epoxide contains a three-tom, cyclic ether as a functional group. The simple...
Pre-lab Questions 1. An epoxide contains a three-tom, cyclic ether as a functional group. The simple po thylene aide h property of you. This makes the carbonched to the yout mack. This is followed by a proto transfer stap Fin the missing products for the following diagram Gachong You should tama mencophesused as reagere. The stone is done by the c coded to you fore out the be o lor 2. Draw the detailed, arrow pushing mechanism for the epoxidation...
organic chemistry II lab help 1-4 plz Post-Lab Questions 1. Give the products from the following...
organic chemistry II lab help 1-4 plz
Post-Lab Questions 1. Give the products from the following reactions Nabi CHOM Nath CH, OH 2. What key IR and NMR absorptions would allow you to determine that the products from the reactions above have been successfully synthesized? Ignore absorption also found in the reactant 3. Nal, usually reacts slowly or not at all with esters. Therefore, LiAlH, is often needed to reduce esters. Why do you think LiAiH, is more reactive than...
I need help with this post lab from Orgo. Anyone please help me. I have included...
I need help with this post lab from Orgo. Anyone please help
me. I have included the procedure from experiment, but let me know
if there is anything to add on this. Thank you
1. Write the overall balanced chemical equation (not the mechanism) for the reaction you carried out in this experiment. Equation must be charge and mass balanced. Use structures not molecular formula. (3 pts) Part A Table 2: Complete this table (15 pts) 2-methyl cyclohexanol cycloalkene Molecular...
Convert playlist Diction QUESTIONS 1. (2 Points) Why is it essential to keep the diazonium salt at zero degrees while you are preparing the sodium 2-naphthoxide solution? 2. (2 Points) Would you need to use sodium carbonate for the diazotization of meta- nitroaniline? Explain your answer. 3. (2 Points) What would be the IUPAC name for the azo dye if you would have used p-chloroaniline instead of sulfanilic acid? Experiment 12 4. (4 Points) Calculate the theoretical yield for Orange...
Please draw the mechanism with the compounds listed below 4
9-4: Transesterification For this assignment, the target compound that you should synthesize is ethyl propionate. This is a carboxylic acid derivative transformation. Keep in mind the mechanism and the potential of reaction reversibility. Examine the product and determine the bond that will be formed. Synthesis Procedures 1. Start Virtual ChemLab and select Transesterification from the list of assignments on the whiteboard. After entering the synthesis laboratory, use the available reagents...
i need all
Post Lab Questions: type in your answers to the following questions Determine what effect the following errors would have on the value for the mass percent water for your hydrate 1. The hydrate was not heated long enough to drive off all the water a. This error will increase decrease leave unchanged the mass in grams for the suminum Eproma after heating b. The error for mass of the aluminum dish Epsom salt after heating that you...
I need help with my pre and post lab questions.
The three compounds below were spotted on a TLC plate and developed to give the TLC plate shown. Which compound corresponds to which spot? Calculate the Rf value for spot B in the TLC plate shown above. When using polarity to determine the relative rates at which organic compounds travel up the TLC plate, we are considering compounds of similar molecular weight. It should also be noted that Rf values...
4:58 4 LTE Object POST-LAB Questions and Image Distance - Thin Lenses NAME JAIME 1. The function of lenses is based on the law of refraction A light beam is traveling from the medium 1 where its speed is V., to the medium 2 where its speed is V2 = 0.8 V, a) If the first medium is the air (n = 1), what is the index of refraction for the second medium? b) If the angle of incidence is...
Please help with pre-lab questions.
Pre-Lab Questions: 1. A sample of 2-butanol has a specific rotation of +3.25. Determine the optical purity (%ee) and percent composition of this sample (see Mohrig section 17.4). The specific rotation of pure (+)-2-butanol is +13.0°. 2. The equation for the formation of the diastereomeric salts is shown in the background information (performed in Part A of the procedure). Write this chemical equation in your notebook, then ALSO write a balanced equation for the formation...
Pre-lab Questions 1. An epoxide contains a three-tom, cyclic ether as a functional group. The simple po thylene aide h property of you. This makes the carbonched to the yout mack. This is followed by a proto transfer stap Fin the missing products for the following diagram Gachong You should tama mencophesused as reagere. The stone is done by the c coded to you fore out the be o lor 2. Draw the detailed, arrow pushing mechanism for the epoxidation...
organic chemistry II lab help 1-4 plz
Post-Lab Questions 1. Give the products from the following reactions Nabi CHOM Nath CH, OH 2. What key IR and NMR absorptions would allow you to determine that the products from the reactions above have been successfully synthesized? Ignore absorption also found in the reactant 3. Nal, usually reacts slowly or not at all with esters. Therefore, LiAlH, is often needed to reduce esters. Why do you think LiAiH, is more reactive than...
I need help with this post lab from Orgo. Anyone please help
me. I have included the procedure from experiment, but let me know
if there is anything to add on this. Thank you
1. Write the overall balanced chemical equation (not the mechanism) for the reaction you carried out in this experiment. Equation must be charge and mass balanced. Use structures not molecular formula. (3 pts) Part A Table 2: Complete this table (15 pts) 2-methyl cyclohexanol cycloalkene Molecular...
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