Homework Answers
Fmoc-Cl is a derivatizing agent (used to alter an analyte). It reacts with glyphosate to form another new compound which absorbs light more strongly than the initial glyphosate compound.
Option B is correct.
Fmoc-Cl is soluble in Dichloromethane while the glyphosate/Fmoc-Cl is water soluble. So dichloromethane is added to separate out Fmoc-Cl from the new compound.
Option A is correct.
Add Answer to:
In the lab procedure, it is necessary to add a reagent to glyphosate called fluorenyl orthochloroformate,...
Based on the Wittig Reaction exp. below, please answer a) and b). In b) you can...
Based on the Wittig Reaction exp. below, please answer a) and
b). In b) you can disregard the part about the IR, just please
interpret and assign protons, shift values, which protons are for
which groups, etc on the HNMR. The % yield was 34%, and MP was
lower than expected (to assist with answering part a). This should
be all the information you need to answer the question.
HNMR
Discuss the percentage yield of the reaction. Explain and provide...
i need help with this lab please. can i get someone to answer the entire thing....
i need help with this lab please. can i get someone to answer
the entire thing. thank you
Instructor Equilibria of Coordination Compounds OBSERVATIONS AND DATA 1. The formation of complex ions with ammonia The net ionic equation for the reaction of excess Cuso, with NH, is 24 Cu2+ + 4NH3 [cu (NH3)4] The predicted effect on the reaction above of adding excess NH, (based on Le Châtelier's principle) is The reaction will shift to the night and product formation...
Experiment Write Up Proposal You will write up a synthesis procedure for one reaction that could...
Experiment Write Up Proposal You will write up a synthesis procedure for one reaction that could be potentially run in a face- to-face Chem 2321 lab session. Your proposal will include an introduction and procedure. The procedure will include step-by-step instructions for running the reaction (including reaction monitoring), work-up. (product isolation and purification), and analysis (characterization). You will need to include sample calculations for percent yield and provide sample spectra analysis. You must upload your proposal as a single document...
The following questions are from an experiment titled Friedel-Crafts Alkylation for Organic Chemistry II Lab. There...
The following questions are from an experiment titled
Friedel-Crafts Alkylation for Organic Chemistry II Lab. There are
pictures attached of the lab manual.
2) Is this method a good route for the preparation of
p-sec-butyltoulene? Give reasons for your answer.
3) Why do you use a large excess of toulene. What are its
functions?
4) What is the purpose for adding the hydrochloric acid to the
water in the separatory funnel in step 5? Hint: If no acid is
added,...
Write a procedure for how to make compounds 7 and 2. NO но. O NaNO2 HCI...
Write a procedure for how to make compounds 7 and 2.
NO но. O NaNO2 HCI (1M, aq) Et EtOHN CH) NaN -OH CH SO H/CHỤC CNC 2, AQSO Acetone Synthetic Procedures To synthesize compound 4. Obtain 0.500 g of 6-hydroxyquinoline and dissolve this solid in a small test tube with 3.0 mL of aqueous 1.0 M HCl. After the entire amount of solid has dissolved cool the solution in an ice bath and add a solution of NaNO, (0.238...
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepa...
i need help with the postlab questions please
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
Attached is the lab experiment. Here are the questions I need help with: 1. What is...
Attached is the lab experiment. Here are the questions I need
help with:
1. What is the purpose of each of the following steps in this
experiment?
a. Adding solid NaCl to the reaction mixture
b. Repeated washings with water, sat'd NAHCO3, and brine
c. the pipet column chromatography
2. Which compound, cyclohexanol or cyclohexanone will have a
higher Rf on a TLC plate?
3. What is the advantage of using sodium hypochlorite as an
oxidant over CrO3 or Na2Cr2O7...
CHEM 242L Exp. 4 Report/ Synthesis of Oil of Wintergreen Name Score: 20 1) Assess the effectivene...
please answer all these questions, thank you.
CHEM 242L Exp. 4 Report/ Synthesis of Oil of Wintergreen Name Score: 20 1) Assess the effectiveness of the experiment and your technique by A) reporting the yield of each step in grams and percent as well as the overall percent yield (What is "overall percent yield?). SHOW ALL CALCULATIONS! B) Give a complete analysis of the identity and purity of your final product and any isolated intermediates 2 What was the purpose...
Exercise 2 Separation of a Mixture Based on Acid-Base Properties One purpose of this exercise is...
Exercise 2 Separation of a Mixture Based on Acid-Base Properties One purpose of this exercise is to learn how to use a separatory funnel to extract a single component away from other compounds in solution. To do so, we will apply the principles of solubility and acid-base behavior you’re seeing in class. One of the compounds is neutral in the acid-base sense. It has no ability to either donate or accept a proton from an aqueous solution, and will remain...
1 - Provide a balanced equation for this reaction 2 - Provide a mechanism for the...
1 - Provide a balanced equation for this reaction
2 - Provide a mechanism for the transformation of cyclohexanol
into cyclohexanone
3 - Provide a flow chart for the workup procedure for isolating
cyclohexane from all the by-products, making sure to note in which
layer you expect to find your product in each extraction.
4 - Provide the theoretical yield of cyclohexane in this
experiment.
PROCEDURE OXIDATION OF CYCLOHEXANOL TO CYCLOHEXANONE Set up a water bath as the heat source...
Based on the Wittig Reaction exp. below, please answer a) and
b). In b) you can disregard the part about the IR, just please
interpret and assign protons, shift values, which protons are for
which groups, etc on the HNMR. The % yield was 34%, and MP was
lower than expected (to assist with answering part a). This should
be all the information you need to answer the question.
HNMR
Discuss the percentage yield of the reaction. Explain and provide...
i need help with this lab please. can i get someone to answer
the entire thing. thank you
Instructor Equilibria of Coordination Compounds OBSERVATIONS AND DATA 1. The formation of complex ions with ammonia The net ionic equation for the reaction of excess Cuso, with NH, is 24 Cu2+ + 4NH3 [cu (NH3)4] The predicted effect on the reaction above of adding excess NH, (based on Le Châtelier's principle) is The reaction will shift to the night and product formation...
Experiment Write Up Proposal You will write up a synthesis procedure for one reaction that could be potentially run in a face- to-face Chem 2321 lab session. Your proposal will include an introduction and procedure. The procedure will include step-by-step instructions for running the reaction (including reaction monitoring), work-up. (product isolation and purification), and analysis (characterization). You will need to include sample calculations for percent yield and provide sample spectra analysis. You must upload your proposal as a single document...
The following questions are from an experiment titled
Friedel-Crafts Alkylation for Organic Chemistry II Lab. There are
pictures attached of the lab manual.
2) Is this method a good route for the preparation of
p-sec-butyltoulene? Give reasons for your answer.
3) Why do you use a large excess of toulene. What are its
functions?
4) What is the purpose for adding the hydrochloric acid to the
water in the separatory funnel in step 5? Hint: If no acid is
added,...
Write a procedure for how to make compounds 7 and 2.
NO но. O NaNO2 HCI (1M, aq) Et EtOHN CH) NaN -OH CH SO H/CHỤC CNC 2, AQSO Acetone Synthetic Procedures To synthesize compound 4. Obtain 0.500 g of 6-hydroxyquinoline and dissolve this solid in a small test tube with 3.0 mL of aqueous 1.0 M HCl. After the entire amount of solid has dissolved cool the solution in an ice bath and add a solution of NaNO, (0.238...
i need help with the postlab questions please
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
Attached is the lab experiment. Here are the questions I need
help with:
1. What is the purpose of each of the following steps in this
experiment?
a. Adding solid NaCl to the reaction mixture
b. Repeated washings with water, sat'd NAHCO3, and brine
c. the pipet column chromatography
2. Which compound, cyclohexanol or cyclohexanone will have a
higher Rf on a TLC plate?
3. What is the advantage of using sodium hypochlorite as an
oxidant over CrO3 or Na2Cr2O7...
please answer all these questions, thank you.
CHEM 242L Exp. 4 Report/ Synthesis of Oil of Wintergreen Name Score: 20 1) Assess the effectiveness of the experiment and your technique by A) reporting the yield of each step in grams and percent as well as the overall percent yield (What is "overall percent yield?). SHOW ALL CALCULATIONS! B) Give a complete analysis of the identity and purity of your final product and any isolated intermediates 2 What was the purpose...
1 - Provide a balanced equation for this reaction
2 - Provide a mechanism for the transformation of cyclohexanol
into cyclohexanone
3 - Provide a flow chart for the workup procedure for isolating
cyclohexane from all the by-products, making sure to note in which
layer you expect to find your product in each extraction.
4 - Provide the theoretical yield of cyclohexane in this
experiment.
PROCEDURE OXIDATION OF CYCLOHEXANOL TO CYCLOHEXANONE Set up a water bath as the heat source...
Most questions answered within 3 hours.
-
A first order chemical reaction has an energy of activation of
90.0 kJ/mol and a rate...
asked 11 minutes ago -
Which statement is not correct?
Mutations change the sequence of nucleotides in DNA.
Mutations can be...
asked 2 hours ago -
An organization is not required to accommodate an employee's
disability when the accommodation would cause "undue...
asked 2 hours ago -
Mojo Mining has a bond outstanding that sells for $2,165 and
matures in 17 years. The...
asked 2 hours ago -
Olympic weightlifter Zoe Smith holds a 58 kg barbell over her
head, 2.1 meters above the...
asked 2 hours ago -
For sample average = 28 and a μ = 17 and a s = 4 and...
asked 2 hours ago -
A
short forward contract that was negotiated some time ago will
expire in three months and...
asked 2 hours ago -
If R = R1L2/L3, what is the measurement error dR based on the
rules of error...
asked 2 hours ago -
At equilibrium, the concentrations of N2(g),
O2 (g) and NO (g) in a sealed reaction vessel...
asked 2 hours ago -
Find P(X-bar > 15.5)
n=81, Mean=15, SD=1
asked 3 hours ago -
3. What percentage of search engine users don’t go to the next
page of search results?...
asked 3 hours ago -
Since Tanya Martin retired, she has used income from her
investment in the Alger Mid Cap...
asked 3 hours ago