None The organic acid benzoic acid will react with the organic base diethylamine.HHa Draw the structures of the products of this neutralization reaction.• All hydrogen atoms are implied, except:•• Hydrogen atoms not attached to carbon atoms• Hydrogen atoms involved in the mechanismApply formal charges where appropriate.Assign lone pairs and radical electrons where appropriate.Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom righ=Separate multiple products using the + sign from the drop-down menu.If needed, use the "starting points" menu to revert to the original molecule(s) shown.?

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Answered: The organic acid benzoic acid will…

Pushing Electrons

4th Edition

ISBN:9781133951889

Author:Weeks, Daniel P.

Publisher:Weeks, Daniel P.

Chapter1: Lewis Structures

Section: Chapter Questions

Problem 13EQ: This is done by removing an unshared pair from each of two adjacent atoms and adding one electron...

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Write an equation for the reaction of CH3 SCH3 with BF3, a Lewis acid, and show by the use of curved arrows how the reaction occurs. • Show all hydrogen atoms that are not attached to a carbon atom. Apply formal charges where appropriate. Assign lone pairs and radical electrons where appropriate. • Use the "starting points" menu to revert to the original molecule(s) shown. • Draw the appropriate electron-flow arrows. • Omit+ signs between structures. ● ● CH3 | :S: | CH3 == starting points == ↑ TAYY : F کر ? ChemDoodleⓇ
The organic acid propanoic acid will react with the organic base cyclohexylamine. *O* H . All hydrogen atoms are implied, except: ● a Draw the structures of the products of this neutralization reaction. H H o Hydrogen atoms not attached to carbon atoms o Hydrogen atoms involved in the mechanism **** Apply formal charges where appropriate. Assign lone pairs and radical electrons where appropriate. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. . Separate multiple products using the + sign from the drop-down menu. ● If needed, use the "starting points" menu to revert to the original molecule(s) shown. ? Sn [F]
Next, let's explore what happens when you remove two hydrogens from the structure above and form ethene, CH,CH,. How many bonds should be between the two carbons to give each carbon a total of four bonds? Draw the structural formula for ethene, CH,CH,.
Click the "draw structure" button to launch the drawing utility. The curved arrow notation is a powerful method used by organic chemists to show the movement of electrons not only in resonance structures, but also in chemical reactions. Since each curved arrow shows the movement of two electrons, following the curved arrows illustrates the bonds that are broken and formed in the reaction. Consider the following reaction. Use the curved arrows drawn in the reaction to draw the structure of X. X is converted in the following step to phenol and HCI. HO H CF + H-CF phenol
Complete the equation for the following proton-transfer reaction by using curved arrows to show the flow of electron pairs and drawing the products of the reaction. • Draw all atoms, including hydrogen atoms. • Apply formal charges where appropriate. Assign lone pairs and radical electrons where appropriate. • Use the "starting points" menu to revert to the original molecule(s) shown. • Draw the appropriate electron-flow arrows. • Omit + signs between structures. 0▾ HH HH == starting points == V H-CI: کر ChemDoodle ?
Draw two additional resonance structures for the following compound. Use curved arrows to show the movement of electrons and draw the resonance hybrid. Note that not all hydrogens and lone pair electrons have been drawn in, it may be helpful to start by drawing those in. Please write your answer on paper and submit it here. If you are not able to submit it here, submit it, along with the other short answer questions, to the "Exam 1 short answer dropbox".
for part b）why do we write AlCl3 at top of the arrow and AlCl4 at the bottom of arrow？？is it any connection between the two？does it means that AlCl 4 need to be present in order to make AlCl3 reacts to the molecule and make the reaction to process？？ 2. why when AlCl3 added，Cl was removed from the ring？what princeiple theory is that ？ 2. when SO3 is added ，SO3 attached to the ring，why ？what principle is behind this phenamonane 3.Just confused about why AlCl3 removes Cl from the ring，while HSO3 donate SO3 to the ring. Is it Something about nucleohilic or eletrciohillic？
Why was the formal charge of (+) placed on this carbon? I understand everything else about the question but can someone help me with explaining this. Thanks!
[Review Topics] [References] Draw a structural formula for 2,2-dimethyl-1-propanol. • 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. opy aste IF
Dd.80.
Complete the equation for the following proton-transfer reaction by using curved arrows to show the flow of electron pairs and drawing the products of the reaction. • Draw all atoms, including hydrogen atoms. Apply formal charges where appropriate. Assign lone pairs and radical electrons where appropriate. • Use the "starting points" menu to revert to the original molecule(s) shown. • Draw the appropriate electron-flow arrows. • Omit + signs between structures. ● ● H-O: == starting points == ↑ TAYY H T H-C-H H-N-H T H در ? ChemDoodle
Please answer all parts. Thanks!

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