RXN curved arrows
Fill in the blanks to describe the curved arrows necessary to make the depicted reaction happen. Begin with the curved arrow that starts in a lower numbered position according to the labeling.
*classification is proton transfer or nucleophilic attack or loss of a leaving group or rearrangement or resonance or N/A
*For curved arrows that are not applicable, enter 0 in both blanks. For instance, if you think this reaction involves only a single curved arrow whose tail is on C-4 and whose head is on C-10 you'd put 4 in the first blank and 10 in the second blank and then 0's in the 3rd and 4th blanks.
the first curved arrow is classified as [A] and starts at starts at [B] and ends at [C]
the second curved arrow is classified as [D] and starts at [E] and ends at [F]
Homework Answers
Answer:
The first curved arrow is classified as Nucleophilic attack and starts at 7 and ends at 5.
The second arrow is classified as N/A and starts at 0 and ends at 0.
RXN curved arrows
page 1.pngpage 2.pngFill in the blanks to describe the curved arrows necessary to make the depicted reaction happen. Begin with the curved arrow that starts in a lower numbered position according to the labeling.*curved arrows are described as proton transfer, nucleophilic attack, loss of a leaving group, resonance, rearrangement, or N/A*For curved arrows that are not applicable, enter 0 in both blanks. For instance, if you think this reaction involves only a single curved arrow whose tail is on C-4 and whose head is on...
This nucleophilic substitution occurs with rearrangement. Draw curved arrows to show the movement of electrons in...
This nucleophilic substitution occurs with
rearrangement. Draw curved arrows to show the movement of electrons
in the following step of the reaction mechanism.
NaOH HON Om This nucleophilic substitution occurs with rearrangement. Draw curved arrows to show the movement of electrons in the following step of the reaction mechanism. Arrow-pushing Instructions Nex mm 34 Submit Answer Try Another Version 1 item attempt remaining
Fill in the appropriate curved mechanism arrows, missing structures, and/or labels for the following reaction. Labels...
Fill in the appropriate curved mechanism arrows,
missing structures, and/or labels for the following reaction.
Labels will either be proton transfer, nucleophilic attack, loss of
leaving group, and
carbonation rearrangement.
.ni 1- nucleophilic attack + OH o OH
curved arrows and equation.
1. For the first equation, predict the organic compound of the reaction. include hydrogen atoms in the reaction.2. Add one or more curved arrows to show the movement of electrons in the second (2) reaction. Use double curved arrow or single barbed arrow appropriately.Add curved arrows for the first step.2.draw both organic and inorganic intermediate species. Include non bonding electrons and charges, where applicable.
b. Use numbers to represent curved arrows to show how the carbocation intermediate reacts with Nu:-...
b. Use numbers to represent curved arrows to show how the carbocation intermediate reacts with Nu:- to form the electrophilic aromatic substitution product. Your first number is atom or bond where the curved arrow starts; your second number is atom or bond where the curved arrow ends. Do not put a comma between your numbers. H I-1 8H7 10 woo + Nu: → CoHJE -1°
b. Use numbers to represent curved arrows to show how the carbocation intermediate reacts with Nur-to...
b. Use numbers to represent curved arrows to show how the carbocation intermediate reacts with Nur-to form the electrophilic aromatic substitution product. Your first number is atom or bond where the curved arrow starts; your second number is atom or bond where the curved arrow ends. Do not put a comma between your numbers. н H. I 8H7 10 19 + Nu: C6H5E Your answer. Do not put a comma between your numbers. Your answer
First box is to add in curved arrows that illustrate the first step of this mechanism....
First box is to add in curved
arrows that illustrate the first step of this mechanism. Second box
is Draw the two intermediates that form and show curved arrows
depicting the next step. Third is Draw the intermediate and the
small molecule with which it will react. Show curved arrows
depicting the next step. Fourth box is Draw the intermediate and
the small molecule with which it will react. Show curved arrows
depicting the next step.
05 Question (1 point)...
First box: draw curved arrows to show protinatuon of the alkene Second box: assign non zero...
First box: draw curved arrows to show protinatuon of the alkene
Second box: assign non zero charges and draw arrows as
necessary to show rearrangement
Third box: assign non zero formal charges
Thank you!
x, draw curved arrows to show protonation of the alkene. In the second box, assign nonzero ement. In the third box, assign nonzero formal charges and draw any necessary arrow(s) to show re formal charges. All necessary atoms and bonds (that is, those that are involved...
1. Provide the products of the reaction below and a detailed reaction mechanism using curved arrows...
1. Provide the products of the reaction below and a detailed reaction mechanism using curved arrows to indicate the movement of electrons. (a) (b) КОН (c) Note that formation of 4- or 7-membered rings is disfavored. Hiyo KOH acidie workup 2. An interesting problem that involves a bit of review (imines and Grignard chemistry) and application of what you previously learned to a new reaction: The Carbon of an imine functional group (i.e. R.C-NR) is sufficiently electron deficient to be...
+ H+ Electrophilic aromatic substitution is a two-step process. In the first step an electrophile, here...
+ H+ Electrophilic aromatic substitution is a two-step process. In the first step an electrophile, here generically shown as Y , reacts with the aromatic ring to form a resonance-stabilized carbocation intermediate. In the second step, loss of a proton from the site of attack restores aromaticity to the ring and completes the reaction. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions no XT + H H- A
This nucleophilic substitution occurs with
rearrangement. Draw curved arrows to show the movement of electrons
in the following step of the reaction mechanism.
NaOH HON Om This nucleophilic substitution occurs with rearrangement. Draw curved arrows to show the movement of electrons in the following step of the reaction mechanism. Arrow-pushing Instructions Nex mm 34 Submit Answer Try Another Version 1 item attempt remaining
Fill in the appropriate curved mechanism arrows,
missing structures, and/or labels for the following reaction.
Labels will either be proton transfer, nucleophilic attack, loss of
leaving group, and
carbonation rearrangement.
.ni 1- nucleophilic attack + OH o OH
b. Use numbers to represent curved arrows to show how the carbocation intermediate reacts with Nu:- to form the electrophilic aromatic substitution product. Your first number is atom or bond where the curved arrow starts; your second number is atom or bond where the curved arrow ends. Do not put a comma between your numbers. H I-1 8H7 10 woo + Nu: → CoHJE -1°
b. Use numbers to represent curved arrows to show how the carbocation intermediate reacts with Nur-to form the electrophilic aromatic substitution product. Your first number is atom or bond where the curved arrow starts; your second number is atom or bond where the curved arrow ends. Do not put a comma between your numbers. н H. I 8H7 10 19 + Nu: C6H5E Your answer. Do not put a comma between your numbers. Your answer
First box is to add in curved
arrows that illustrate the first step of this mechanism. Second box
is Draw the two intermediates that form and show curved arrows
depicting the next step. Third is Draw the intermediate and the
small molecule with which it will react. Show curved arrows
depicting the next step. Fourth box is Draw the intermediate and
the small molecule with which it will react. Show curved arrows
depicting the next step.
05 Question (1 point)...
First box: draw curved arrows to show protinatuon of the alkene
Second box: assign non zero charges and draw arrows as
necessary to show rearrangement
Third box: assign non zero formal charges
Thank you!
x, draw curved arrows to show protonation of the alkene. In the second box, assign nonzero ement. In the third box, assign nonzero formal charges and draw any necessary arrow(s) to show re formal charges. All necessary atoms and bonds (that is, those that are involved...
1. Provide the products of the reaction below and a detailed reaction mechanism using curved arrows to indicate the movement of electrons. (a) (b) КОН (c) Note that formation of 4- or 7-membered rings is disfavored. Hiyo KOH acidie workup 2. An interesting problem that involves a bit of review (imines and Grignard chemistry) and application of what you previously learned to a new reaction: The Carbon of an imine functional group (i.e. R.C-NR) is sufficiently electron deficient to be...
+ H+ Electrophilic aromatic substitution is a two-step process. In the first step an electrophile, here generically shown as Y , reacts with the aromatic ring to form a resonance-stabilized carbocation intermediate. In the second step, loss of a proton from the site of attack restores aromaticity to the ring and completes the reaction. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions no XT + H H- A
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