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Please help how to synthesize the product from given starting
compounds with shortest step as possible....
please help to synthesize the product from the starting compounds with the shortest steps as possible....
please help to synthesize the product from the starting
compounds with the shortest steps as possible. Thank you.
он В) С) D) но. E)
02. Synthesize the following product from the given starting compounds. This will require more than one...
02. Synthesize the following product from the given starting compounds. This will require more than one step. You may use any organic or inorganic reagent to carry out this synthesis. (8 pts each) (you can also use any one C reagent)
Q2. Synthesize the following product from the given starting compounds. This will require more than one...
Q2. Synthesize the following product from the given starting compounds. This will require more than one step. You may use any organic or inorganic reagent to carry out this synthesis. (8 pts each) Do (you can also use any one C reagent) ОН (you can also use any two carbon reagent)
I need help with #2 please explain step by step. POST LAB QUESTIONS 1. Predict all possible bromination products of...
I need help with #2 please explain step by step.
POST LAB QUESTIONS 1. Predict all possible bromination products of the following substrate using the above reaction conditions. Show stereochemistry (i.e. dashed and wedged bonds, and label chiral centers (R or S), if necessary. Dogou or dilbi o bando sobre in the manica Br2 YCHE CH3 2. A researcher performs the above reaction starting with 0.150 g of the alkene substrate, 0.375 g of pyridinium tribromide, and 2.00 mL of...
Please explain what is going on in this lab for STEP 3. what are some important...
Please explain what is going on in this lab for STEP 3. what
are some important factors?
Multistep Synthesis Preparation of 4,4-Diphenyl-3-buten-2-one! This experiment illustrates se multistep synthesis, in which the the next. This process is very common iment illustrates several important concepts of organic synthesis. It is a synthesis, in which the product of one reaction becomes the starting material of This process is very common in industry and research, and demands careful to vields and techniques. The experiment...
use the notes provided to help answer the question above. will rate well The second step...
use the notes provided to help answer the question
above. will rate well
The second step of the synthesis transformation of the chlorosulfonyl functional group into a sulfonamide) is an example of a a. Nucleophilic displacement (substitution) b Elimination C. Electrophilic aromatic substitution d. Acid hydrolysis Esterification e. THE SULFONIC ACID GROUP AND ITS DERIVATIVES Sulfonic acids are organic analogs of sulfuric acid, a very strong acid. They are highly corrosive, react vigorously with water, and can cause skin bums....
What is the theoretical yield (in grams) and percent yield of your triphenylmethanol product in this...
What is the theoretical yield (in grams) and percent yield of your
triphenylmethanol product in this experiment? (Weight of
triphenylmethanol: 0.060g)
BACKGROUND AND THEORY The Grignard reaction was one of the first organometallic reactions discovered and is still one of the most useful synthetically. By reacting an organohalide (usually a bromide) with magnesium in ethereal solvent, carbon becomes a nucleophile. Grignard reagents are the starting points for the syntheses of many alkanes, primary, secondary, and tertiary alcohols, alkenes, and carboxylic...
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,...
help with identifiying each unknown in extraction and washing experiment. the ir spectra are given below,...
help with identifiying each unknown in extraction and washing
experiment. the ir spectra are given below, along with data, and
the lab sheet is attached.
Neutral Solid Primary amine (Aniline) 3403cm - NE presence Transmittance 60 3258cm 1 streren NOUD Streich 50 Ctretcher strator NH2 aromatto 11 NO2 aring 2-nitroaniline K LILI 3600 3200 2800 2400 2000 1800 1600 Wavenumber cm-1 1400 1200 1000 800 600 Basic Solid primary amine Transmittance I NH2 Stretch p-acetvianiline 70 60 CS HG NO...
please identify the unknown and write a derivative Unknown compound 3 Clear liquid Physcial Properties Solubility...
please identify the unknown and write a derivative
Unknown compound 3 Clear liquid Physcial Properties Solubility Dissolve in ethyl ether Not dissolved in water Boiling point 77 IR spectrum Transmitance 3000 1000 2000 Wavenumber cm-1) Classification Positive test in Alkaline Iron (III) Hydroxamate test test CLASSIFICATION TESTS These tests must be done together with known AND FOLLOW PROCEDURE IN YOUR TEXT CARBOXYLIC ACIDS are detected by teating aqueous solutions with limus or pH paper. Also, disolve In NaHCO with bubbles...
please help to synthesize the product from the starting
compounds with the shortest steps as possible. Thank you.
он В) С) D) но. E)
02. Synthesize the following product from the given starting compounds. This will require more than one step. You may use any organic or inorganic reagent to carry out this synthesis. (8 pts each) (you can also use any one C reagent)
Q2. Synthesize the following product from the given starting compounds. This will require more than one step. You may use any organic or inorganic reagent to carry out this synthesis. (8 pts each) Do (you can also use any one C reagent) ОН (you can also use any two carbon reagent)
I need help with #2 please explain step by step.
POST LAB QUESTIONS 1. Predict all possible bromination products of the following substrate using the above reaction conditions. Show stereochemistry (i.e. dashed and wedged bonds, and label chiral centers (R or S), if necessary. Dogou or dilbi o bando sobre in the manica Br2 YCHE CH3 2. A researcher performs the above reaction starting with 0.150 g of the alkene substrate, 0.375 g of pyridinium tribromide, and 2.00 mL of...
Please explain what is going on in this lab for STEP 3. what
are some important factors?
Multistep Synthesis Preparation of 4,4-Diphenyl-3-buten-2-one! This experiment illustrates se multistep synthesis, in which the the next. This process is very common iment illustrates several important concepts of organic synthesis. It is a synthesis, in which the product of one reaction becomes the starting material of This process is very common in industry and research, and demands careful to vields and techniques. The experiment...
use the notes provided to help answer the question
above. will rate well
The second step of the synthesis transformation of the chlorosulfonyl functional group into a sulfonamide) is an example of a a. Nucleophilic displacement (substitution) b Elimination C. Electrophilic aromatic substitution d. Acid hydrolysis Esterification e. THE SULFONIC ACID GROUP AND ITS DERIVATIVES Sulfonic acids are organic analogs of sulfuric acid, a very strong acid. They are highly corrosive, react vigorously with water, and can cause skin bums....
What is the theoretical yield (in grams) and percent yield of your
triphenylmethanol product in this experiment? (Weight of
triphenylmethanol: 0.060g)
BACKGROUND AND THEORY The Grignard reaction was one of the first organometallic reactions discovered and is still one of the most useful synthetically. By reacting an organohalide (usually a bromide) with magnesium in ethereal solvent, carbon becomes a nucleophile. Grignard reagents are the starting points for the syntheses of many alkanes, primary, secondary, and tertiary alcohols, alkenes, and carboxylic...
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,...
help with identifiying each unknown in extraction and washing
experiment. the ir spectra are given below, along with data, and
the lab sheet is attached.
Neutral Solid Primary amine (Aniline) 3403cm - NE presence Transmittance 60 3258cm 1 streren NOUD Streich 50 Ctretcher strator NH2 aromatto 11 NO2 aring 2-nitroaniline K LILI 3600 3200 2800 2400 2000 1800 1600 Wavenumber cm-1 1400 1200 1000 800 600 Basic Solid primary amine Transmittance I NH2 Stretch p-acetvianiline 70 60 CS HG NO...
please identify the unknown and write a derivative
Unknown compound 3 Clear liquid Physcial Properties Solubility Dissolve in ethyl ether Not dissolved in water Boiling point 77 IR spectrum Transmitance 3000 1000 2000 Wavenumber cm-1) Classification Positive test in Alkaline Iron (III) Hydroxamate test test CLASSIFICATION TESTS These tests must be done together with known AND FOLLOW PROCEDURE IN YOUR TEXT CARBOXYLIC ACIDS are detected by teating aqueous solutions with limus or pH paper. Also, disolve In NaHCO with bubbles...
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H0:μ=56.9
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