Homework Answers
As per HomeworkLib policy only first question is answered in case of multiple question.
Add Answer to:
i get to the product but always add 6 carbons! how do i make
it with...
How do you make 3-cyclopentane-1-propanal with starting reactants composed of only 6 carbons or less? I'm...
How do you make 3-cyclopentane-1-propanal with starting reactants composed of only 6 carbons or less? I'm confused about how to synthesize the compound. Explanation about why the specific reagents are chosen would be appreciated!
5. Starting with a compound having no more than 6 carbons make the given molecules following...
5. Starting with a compound having no more than 6 carbons make the given molecules following the specific instructions for each one. While mechanisms are not needed here, please make sure you write out the reagents and products of every step. (5 x 5) a. Use a Grignard reaction in one of the steps OH b. Use the Gilmann reagent in one of the steps
5. Starting with a compound having no more than 6 carbons make the given molecules following...
5. Starting with a compound having no more than 6 carbons make the given molecules following the specific instructions for each one. While mechanisms are not needed here, please make sure you write out the reagents and products of every step. (5 5) a. Use a Grignard reaction in one of the steps OH b. Use the Gilmann reagent in one of the steps
Synthesize the following compounds from the given starting material. You can add on any alkyl/ alkyl...
Synthesize the following compounds from the given starting
material. You can add on any alkyl/ alkyl halide under 6 carbons or
any necessary inorganic reagent needed (this includes triphenyl
phosphine (Ph3P). Please draw all intermediates and
reagents necessary to get to the product.
OH سالن سل = ها را
① ( 38 Points) Synthesis for the cases below show how you would synthesize the desired...
① ( 38 Points) Synthesis for the cases below show how you would synthesize the desired product from the given starting material using any Reaction in Chapters 1-9, Use any recessary Reagents and any alcohol up to 6 carbons H-C=C-17 myh Acetylene Starting material heptanal starting maker
Which starting matrial, solvent and reagent should I use to get 1-phenyl-1-propanol? Grignard Addition VCL 10-1:...
Which starting matrial, solvent and reagent should I use to
get 1-phenyl-1-propanol?
Grignard Addition VCL 10-1: Grignard Addition - 1 For this assignment, the target compound that you should synthesize is 1-phenyl-1-propanol. This is an organometallic addition reaction. Examine the product and identify potential bonds that may be formed. Keep in mind the mechanism and the need to quench the reaction with acid to liberate the neutral product. Synthesis Procedures 1. Start Virtual ChemLab and select Grignard Addition - /...
1. Show how you could make the amine shown by Reductive Amination and by Acylation and...
1. Show how you could make the amine shown by Reductive Amination and by Acylation and then reduction. Clearly show the starting materials and reagents for each approach Q Target amine: 2. Devise a synthesis of the target amine from question one starting from Toluene (methyl benzene) and any two carbon compounds you wish. 3. Propose a synthesis of this azo dye starting from Benzene and acetic acid as your only source of carbons. Target Dye: 4. Can you rationalize...
what are the starting matrial, solvent, and reagent to use to get 1-phenyl-1-propanol? Grignard Addition VCL...
what are the starting matrial, solvent, and reagent to use to
get 1-phenyl-1-propanol?
Grignard Addition VCL 10-1: Grignard Addition - 1 For this assignment, the target compound that you should synthesize is 1-phenyl-1-propanol. This is an organometallic addition reaction. Examine the product and identify potential bonds that may be formed. Keep in mind the mechanism and the need to quench the reaction with acid to liberate the neutral product. Synthesis Procedures 1. Start Virtual ChemLab and select Grignard Addition -/...
S. Show how you would prepare the following compound using an organometallic reagent. You may use...
S. Show how you would prepare the following compound using an organometallic reagent. You may use any hydrocarbons, organohalides, alcohols and/or carbonyl compounds that have five of fewer carbon atoms You may also use any needed reagents and solvents OH This one as well. He quits grading when you get two mistakes. 6. Propose a synthesis of the following compound using a Wittig reaction. You may use triphenylphosphine (Ph P) and any reagents containing five carbons or less as starting...
1-24 need help really lost Proton Transfer: deprotonation D. 1) Add the appropriate curved arrows for...
1-24 need help really lost
Proton Transfer: deprotonation D. 1) Add the appropriate curved arrows for the following deprotonation step. Also add the other product notice how the Tema s can be converted to this by use of a strong base such as sodium a sodium ion (Na) is not drawn, in this case it is just a spectatorio PCW27 - Mechanistic steps - Part Name: Time spent 2) Label the above compounds with the appropriate name from the previous...
5. Starting with a compound having no more than 6 carbons make the given molecules following the specific instructions for each one. While mechanisms are not needed here, please make sure you write out the reagents and products of every step. (5 x 5) a. Use a Grignard reaction in one of the steps OH b. Use the Gilmann reagent in one of the steps
5. Starting with a compound having no more than 6 carbons make the given molecules following the specific instructions for each one. While mechanisms are not needed here, please make sure you write out the reagents and products of every step. (5 5) a. Use a Grignard reaction in one of the steps OH b. Use the Gilmann reagent in one of the steps
Synthesize the following compounds from the given starting
material. You can add on any alkyl/ alkyl halide under 6 carbons or
any necessary inorganic reagent needed (this includes triphenyl
phosphine (Ph3P). Please draw all intermediates and
reagents necessary to get to the product.
OH سالن سل = ها را
① ( 38 Points) Synthesis for the cases below show how you would synthesize the desired product from the given starting material using any Reaction in Chapters 1-9, Use any recessary Reagents and any alcohol up to 6 carbons H-C=C-17 myh Acetylene Starting material heptanal starting maker
Which starting matrial, solvent and reagent should I use to
get 1-phenyl-1-propanol?
Grignard Addition VCL 10-1: Grignard Addition - 1 For this assignment, the target compound that you should synthesize is 1-phenyl-1-propanol. This is an organometallic addition reaction. Examine the product and identify potential bonds that may be formed. Keep in mind the mechanism and the need to quench the reaction with acid to liberate the neutral product. Synthesis Procedures 1. Start Virtual ChemLab and select Grignard Addition - /...
1. Show how you could make the amine shown by Reductive Amination and by Acylation and then reduction. Clearly show the starting materials and reagents for each approach Q Target amine: 2. Devise a synthesis of the target amine from question one starting from Toluene (methyl benzene) and any two carbon compounds you wish. 3. Propose a synthesis of this azo dye starting from Benzene and acetic acid as your only source of carbons. Target Dye: 4. Can you rationalize...
what are the starting matrial, solvent, and reagent to use to
get 1-phenyl-1-propanol?
Grignard Addition VCL 10-1: Grignard Addition - 1 For this assignment, the target compound that you should synthesize is 1-phenyl-1-propanol. This is an organometallic addition reaction. Examine the product and identify potential bonds that may be formed. Keep in mind the mechanism and the need to quench the reaction with acid to liberate the neutral product. Synthesis Procedures 1. Start Virtual ChemLab and select Grignard Addition -/...
S. Show how you would prepare the following compound using an organometallic reagent. You may use any hydrocarbons, organohalides, alcohols and/or carbonyl compounds that have five of fewer carbon atoms You may also use any needed reagents and solvents OH This one as well. He quits grading when you get two mistakes. 6. Propose a synthesis of the following compound using a Wittig reaction. You may use triphenylphosphine (Ph P) and any reagents containing five carbons or less as starting...
1-24 need help really lost
Proton Transfer: deprotonation D. 1) Add the appropriate curved arrows for the following deprotonation step. Also add the other product notice how the Tema s can be converted to this by use of a strong base such as sodium a sodium ion (Na) is not drawn, in this case it is just a spectatorio PCW27 - Mechanistic steps - Part Name: Time spent 2) Label the above compounds with the appropriate name from the previous...
Most questions answered within 3 hours.
-
Q4. Company director dies of brain hemorrhage after heading a
football. David Belk, 50, of Macclesfield,...
asked 1 hour ago -
If this 2.0 ppm dilution is still measurable, the detection
limit for STD-B is less than...
asked 1 hour ago -
Calculate the ideal banking angle in degrees for a gentle turn of
1.8 km radius on...
asked 1 hour ago -
From these three classification approaches (decision trees,
Naïve Bayes and neural networks), both with their own...
asked 1 hour ago -
A soda dispenser can be adjusted to deliver any fixed number of
ounces of soft drink....
asked 1 hour ago -
A hockey puck (1) of mass 160 g is shot east at a speed of 6.60...
asked 1 hour ago -
Segregation of duties reduces the opportunities for a person to
be in a position to do...
asked 1 hour ago -
Can an organism use both oxidative phosphorylation and substrate
level phosphorylation? If so, what are some...
asked 1 hour ago -
The masses and coordinates of three spheres are as follows:
12 kg, x = 0.50 m,...
asked 1 hour ago -
Problem 1: A cell generates a traction force of 2×〖10〗^4
μ"dynes" and travels at a speed...
asked 1 hour ago -
How can a company with future income of 152 billion but 4.5
billion in debt overcome...
asked 1 hour ago -
Ryman Healthcare stock is trading at $13. Every six months, they
pay a 15 cent dividend....
asked 1 hour ago