*PLEASE ANSWER THESE QUESTIONS CORRECTLY. IT'S FOR AN EXAM*
*THIS WAS THE WRONG ANSWER*
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*PLEASE ANSWER THESE QUESTIONS CORRECTLY. IT'S FOR AN
EXAM*
*THIS WAS THE WRONG ANSWER*
Predict the...
1. Predict the major products of the following reactions. (Hint: draw out Tosylate ion) ethyl tosylate...
1. Predict the major products of the following reactions. (Hint: draw out Tosylate ion) ethyl tosylate + potassium tert-butoxide 2.isobutyl tosylate + NaI 3.(R)-2-hexyl tosylate + NaCN (show sterochemistry) 4.the tosylate of cyclohexylmethanol + excess NH3 5.n-butyl tosylate + sodium acetylide, H−C≡C:−Na+
*PLEASE ANSWER THESE QUESTIONS CORRECTLY. IT'S FOR AN EXAM* Predict the major products of the following...
*PLEASE ANSWER THESE QUESTIONS CORRECTLY. IT'S FOR AN
EXAM*
Predict the major products of the following reactions. (Hint draw out Tosylate ion) Part D the tosylate of cyclohexylmethanol + excess NH3 Part E n-butyl tosylate + sodium acetylide, H-C=C: Na
please help ! answer all quetions for the 8 photos thank you! Review Constants Periodic Table...
please help ! answer all quetions for the 8 photos thank
you!
Review Constants Periodic Table Part B Give the IUPAC name of the carboxylic acid and the alcohol used to prepare methyl butanoate. Spell out the full IUPAC names of the carboxylic acid and alcohol separated by a comma. Submit Request Answer Part C Enter a balanced equation for the acid hydrolysis of methyl butanoate. (Use either molecular formulas or condensed structural formulas, but be consistent in your equation.)...
It's telling me that this is incorrect... What is the correct answer if this is not?...
It's telling me that this is incorrect... What is the correct
answer if this is not? Please help by clearly giving the correct
answer followed by an explanation if you wish. I have posted this
already but the first response I got was too messy and didn't
clearly show the answer. Thank you!
Heat CH3-CH2-C-OH + O Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Adva bond is active by default. Include...
I need two products and I am not sure what I am getting wrong. Problem 8.46 (c) Predict the major products of the tollowing reaction, and give the structures of any intermediates. Include stereochemi...
I need two products and I am not sure what I am getting
wrong.
Problem 8.46 (c) Predict the major products of the tollowing reaction, and give the structures of any intermediates. Include stereochemistry where appropriate. CH2 (1) BH3 THF (2) H2O2, OH Draw the molecules on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars, including charges where needed. The single bond is active by default. Show the appropriate stereochemistry by choosing the...
I have drawn this, but it says its wrong. I think I'm missing a stereoisomer, but...
I have drawn this, but it says
its wrong. I think I'm missing a stereoisomer, but I don't know how
to draw it.
What stereoisomers are obtained from the reaction of each of the following the alkenes with a peroxyacid followed by reaction with hydroxide ion? Part A trans-2-pentene Draw the molecule(s) on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. Sho stereochemistry by choosing the dashed or wedged buttons and then clicking...
please help The dehydration of alcohols Under acidic conditions, alcohols will undergo a dehydration reaction, producing...
please help
The dehydration of alcohols Under acidic conditions, alcohols will undergo a dehydration reaction, producing an alkene and water. During the reaction, the hydroxyl group of the alcohol and a hydrogen atom from an adjacent carbon atom are lost. The reaction takes place in three steps, as shown in the diagram. (Figure 1) In the first step, a hydrogen lon bonds to the hydroxyl group of the alcohol. In the second step, the protonated hydroxl group leaves the compound,...
please help me figure out why my answer is wrong. thanks <Chapter 12-2 Problem 12.51 Review...
please help me figure out why my answer is wrong. thanks
<Chapter 12-2 Problem 12.51 Review Constants Periodic Table Draw the condensed structural or line-angle formula for the aliene, aldehyde, or ketone product of each of the following reactions ОН CH-CH-CH-CH-CH, H", loa , Draw the molecule on the canvas by choosing buttons from the Tools for bonda) Atoms, and Advanced Template toolbars The single bond is active by default. D HE POO
please answer it correctly as I posted it before and it's wrong. Running on a treadmill...
please answer it correctly as
I posted it before and it's wrong.
Running on a treadmill is slightly easier than running outside because there is no drag force to work against. Suppose a 60 kg runner completes a 5.0 km race in 20 minutes. Part A Determine the drag force on the runner during the race. Suppose that the cross section area of the runner is 0.72 m² Express your answer with the appropriate units. UA ? D = Value...
*PLEASE ANSWER THESE QUESTIONS CORRECTLY. IT'S FOR AN
EXAM*
Predict the major products of the following reactions. (Hint draw out Tosylate ion) Part D the tosylate of cyclohexylmethanol + excess NH3 Part E n-butyl tosylate + sodium acetylide, H-C=C: Na
please help ! answer all quetions for the 8 photos thank
you!
Review Constants Periodic Table Part B Give the IUPAC name of the carboxylic acid and the alcohol used to prepare methyl butanoate. Spell out the full IUPAC names of the carboxylic acid and alcohol separated by a comma. Submit Request Answer Part C Enter a balanced equation for the acid hydrolysis of methyl butanoate. (Use either molecular formulas or condensed structural formulas, but be consistent in your equation.)...
It's telling me that this is incorrect... What is the correct
answer if this is not? Please help by clearly giving the correct
answer followed by an explanation if you wish. I have posted this
already but the first response I got was too messy and didn't
clearly show the answer. Thank you!
Heat CH3-CH2-C-OH + O Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Adva bond is active by default. Include...
I need two products and I am not sure what I am getting
wrong.
Problem 8.46 (c) Predict the major products of the tollowing reaction, and give the structures of any intermediates. Include stereochemistry where appropriate. CH2 (1) BH3 THF (2) H2O2, OH Draw the molecules on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars, including charges where needed. The single bond is active by default. Show the appropriate stereochemistry by choosing the...
I have drawn this, but it says
its wrong. I think I'm missing a stereoisomer, but I don't know how
to draw it.
What stereoisomers are obtained from the reaction of each of the following the alkenes with a peroxyacid followed by reaction with hydroxide ion? Part A trans-2-pentene Draw the molecule(s) on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. Sho stereochemistry by choosing the dashed or wedged buttons and then clicking...
please help
The dehydration of alcohols Under acidic conditions, alcohols will undergo a dehydration reaction, producing an alkene and water. During the reaction, the hydroxyl group of the alcohol and a hydrogen atom from an adjacent carbon atom are lost. The reaction takes place in three steps, as shown in the diagram. (Figure 1) In the first step, a hydrogen lon bonds to the hydroxyl group of the alcohol. In the second step, the protonated hydroxl group leaves the compound,...
please help me figure out why my answer is wrong. thanks
<Chapter 12-2 Problem 12.51 Review Constants Periodic Table Draw the condensed structural or line-angle formula for the aliene, aldehyde, or ketone product of each of the following reactions ОН CH-CH-CH-CH-CH, H", loa , Draw the molecule on the canvas by choosing buttons from the Tools for bonda) Atoms, and Advanced Template toolbars The single bond is active by default. D HE POO
please answer it correctly as
I posted it before and it's wrong.
Running on a treadmill is slightly easier than running outside because there is no drag force to work against. Suppose a 60 kg runner completes a 5.0 km race in 20 minutes. Part A Determine the drag force on the runner during the race. Suppose that the cross section area of the runner is 0.72 m² Express your answer with the appropriate units. UA ? D = Value...
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