please don't use any
abbreviations!
Homework Answers
Add Answer to:
please don't use any
abbreviations!
The following structure represents an intermediate formed by addition of an...
The following structure represents an intermediate formed by addition of an ester enolate ion to a...
The following structure represents an intermediate formed by addition of an ester enolate ion to a second ester molecule. Draw the reactant. ball & stick Blabels • You do not have to consider stereochemistry, • You do not have to explicitly draw Hatoms. • Do not include lone pairs in your answer. They will not be considered in the grading С P 012 <
please don't use any abbreviations! like I don't know how to draw anything like oet or...
please don't use any abbreviations! like I
don't know how to draw anything like oet or an R group like please
just draw out the whole thing!
CH3 CO2Et Hagemann's ester The compound known as Hagemann's ester is prepared by treatment of a mixture of formaldehyde and ethyl acetoacetate with base, followed by acid-catalyzed decarboxylation. The reaction involves the following steps: 1. Deprotonation of ethyl acetoacetate to form enolate ion 1; 2. Reaction of the enolate ion with formaldehyde to...
please don't use any abbreviations! like I don't know how to draw anything like oet or...
please don't use any
abbreviations! like I don't know how to draw anything like oet or
an R group like please just draw out the whole thing!
NaOH ethanol HO This reaction involves an intramolecular Michael reaction followed by an intramolecular aldol reaction. The steps involved are as follows: 1. Deprotonation to form enolate ion 1; 2. Cyclization via an intramolecular Michael reaction to form intermediate 2; 3. Deprotonation to form enolate ion 3; 4. Intramolecular aldol cyclization to form...
Draw the structure of the polymer that could be made from the following monomer. ball &...
Draw the structure of the polymer that could be made from the following monomer. ball & stick labels You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. Do not include lone pairs in your answer. They will not be considered in the grading. In cases where there is more than one answer, just draw one Use R1 groups to indicate the points where the polymer repeats. The R group tool is located in...
Homework marked this wrong. Not sure what I did wrong Nat -OET ethanol This reaction involves...
Homework marked this wrong. Not sure what I did wrong
Nat -OET ethanol This reaction involves two successive Michael reactions, and has the following steps: 1. Deprotonation forms enolate ion 1; 2. The first Michael reaction forms enolate ion 2; 3. The second Michael reaction forms enolate ion 3; 4. Protonation leads to the final product. Write the mechanism out on a sheet of paper, and then draw the structure of enolate ion 2. • You do not have to...
Draw the aldehyde or ketone that the following enone could be prepared from by the aldol...
Draw the aldehyde or ketone that the following enone could be prepared from by the aldol reaction. TI FI 13 ball & stick labels • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. . Do not include lone pairs in your answer. They will not be considered in the grading. • In cases where there is more than one answer, just draw one. С ору P C (1
The double cyclization (above) proceeds by formation of an enolate followed by two successive intramolecular Michael...
The double cyclization (above) proceeds by formation of an enolate followed by two successive intramolecular Michael reactions. Write a detailed mechanism for this reaction on paper, then draw structural formulas for the reactant enolate and adduct enolate of the first Michael reaction in the window below. You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. Do not include lone pairs in your answer. They will not be considered in the grading. Draw enolates...
During electrophilic aromatic substitution, a resonance-stabilized cation intermediate is formed. Groups, already present on the benzene...
During electrophilic aromatic substitution, a resonance-stabilized cation intermediate is formed. Groups, already present on the benzene ring, that direct ortho/para further stabilize this intermediate by participating in the resonance delocalization of the positive charge. Assume that the following group is present on a benzene ring at position 1 and that you are brominating the ring at positon 4. In the box below draw the structure of the resonance contributor that shows this group actively participating in the charge delocalization. -OCH3...
Draw the structure of the major organic product of the following reaction. Predict whether the product...
Draw the structure of the major organic product of the following reaction. Predict whether the product will be an aldol or an enone. 10% aqueous NaOH 25° You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. Do not include lone pairs in your answer. They will not be considered in the grading. .If no reaction occurs, draw the organic starting material C P astered
The following model represents the carbocation intermediate formed in the addition reaction of HBr to two...
The following model represents the carbocation intermediate formed in the addition reaction of HBr to two different alkenes. Draw structures for both alkenes. wireframe M - + labels • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures with + signs from the drop-down menu.
The following structure represents an intermediate formed by addition of an ester enolate ion to a second ester molecule. Draw the reactant. ball & stick Blabels • You do not have to consider stereochemistry, • You do not have to explicitly draw Hatoms. • Do not include lone pairs in your answer. They will not be considered in the grading С P 012 <
please don't use any abbreviations! like I
don't know how to draw anything like oet or an R group like please
just draw out the whole thing!
CH3 CO2Et Hagemann's ester The compound known as Hagemann's ester is prepared by treatment of a mixture of formaldehyde and ethyl acetoacetate with base, followed by acid-catalyzed decarboxylation. The reaction involves the following steps: 1. Deprotonation of ethyl acetoacetate to form enolate ion 1; 2. Reaction of the enolate ion with formaldehyde to...
please don't use any
abbreviations! like I don't know how to draw anything like oet or
an R group like please just draw out the whole thing!
NaOH ethanol HO This reaction involves an intramolecular Michael reaction followed by an intramolecular aldol reaction. The steps involved are as follows: 1. Deprotonation to form enolate ion 1; 2. Cyclization via an intramolecular Michael reaction to form intermediate 2; 3. Deprotonation to form enolate ion 3; 4. Intramolecular aldol cyclization to form...
Draw the structure of the polymer that could be made from the following monomer. ball & stick labels You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. Do not include lone pairs in your answer. They will not be considered in the grading. In cases where there is more than one answer, just draw one Use R1 groups to indicate the points where the polymer repeats. The R group tool is located in...
Homework marked this wrong. Not sure what I did wrong
Nat -OET ethanol This reaction involves two successive Michael reactions, and has the following steps: 1. Deprotonation forms enolate ion 1; 2. The first Michael reaction forms enolate ion 2; 3. The second Michael reaction forms enolate ion 3; 4. Protonation leads to the final product. Write the mechanism out on a sheet of paper, and then draw the structure of enolate ion 2. • You do not have to...
Draw the aldehyde or ketone that the following enone could be prepared from by the aldol reaction. TI FI 13 ball & stick labels • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. . Do not include lone pairs in your answer. They will not be considered in the grading. • In cases where there is more than one answer, just draw one. С ору P C (1
The double cyclization (above) proceeds by formation of an enolate followed by two successive intramolecular Michael reactions. Write a detailed mechanism for this reaction on paper, then draw structural formulas for the reactant enolate and adduct enolate of the first Michael reaction in the window below. You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. Do not include lone pairs in your answer. They will not be considered in the grading. Draw enolates...
During electrophilic aromatic substitution, a resonance-stabilized cation intermediate is formed. Groups, already present on the benzene ring, that direct ortho/para further stabilize this intermediate by participating in the resonance delocalization of the positive charge. Assume that the following group is present on a benzene ring at position 1 and that you are brominating the ring at positon 4. In the box below draw the structure of the resonance contributor that shows this group actively participating in the charge delocalization. -OCH3...
Draw the structure of the major organic product of the following reaction. Predict whether the product will be an aldol or an enone. 10% aqueous NaOH 25° You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. Do not include lone pairs in your answer. They will not be considered in the grading. .If no reaction occurs, draw the organic starting material C P astered
The following model represents the carbocation intermediate formed in the addition reaction of HBr to two different alkenes. Draw structures for both alkenes. wireframe M - + labels • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures with + signs from the drop-down menu.
Most questions answered within 3 hours.
-
The blues made its way into many kinds of music. Eric Clapton,
The Beatles, and Elvis...
asked 1 hour ago -
8. A wave in a string has a wave function given by: y (x, t) =...
asked 34 minutes ago -
If you’re standing at the bottom of a hill and asked to evaluate
it while being...
asked 2 hours ago -
1. Which region has taken the lead in the world of
e-waste handling?
a) European Union...
asked 2 hours ago -
A 8.15- g bullet from a 9-mm pistol has a velocity of 366.0 m/s.
It strikes...
asked 3 hours ago -
The outstanding bonds of Alpha Extracts have a yield to maturity
of 7.4 percent and a...
asked 3 hours ago -
The Problem: The Case of the Harmonizing Vacations
Your CEO is exploring partnering with a European...
asked 5 hours ago -
A chemical equation is balanced by adding coefficients in front
of some formulas so that the...
asked 5 hours ago -
From the literature (reference your sources): What are the
lattice parameters of calcite and aragonite? Why...
asked 5 hours ago -
Your system is rejecting the question am asking which is
preceded by a case study. It...
asked 5 hours ago -
3. On January 2, 2000, Larry creates a trust with himself as
trustee. Larry as trustee...
asked 5 hours ago -
A member of the volleyball team spikes the ball. During this
process, she changes the velocity...
asked 6 hours ago