7. Use curved arrows to draw (3) additional resonance structures. Start by allowing for the (+) charge on the ring to "move in a clockwise direction." CIRCLE the best resonance contributor and explain your selection.
Q: Draw all significant resonance structures for the following compound:
A: By movement of free electrons through the pi bonds form resonating structures.
Q: Box 1 Box 2 Box 3 HBr Then, complete the figure on your scratch paper by drawing out the…
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Q: Add curved arrows to the following polar reactions to indicate the flow of electrons in each:
A: (a) Chlorine behaves as an electrophilic center and ammonia as a nucleophile.
Q: 3. Rank the rings below from most activated to least activated.
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Q: When drawing the resonance structures for a toluene carbocation (like the one attached below),…
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Q: Which is the stronger acid? A OR B? SEE THE PICTURE BELOW
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Q: Use resonance structures to help you identify all sites of low electron density (õ+) in the…
A: When electrons moves away from the carbon , that carbon carries partial positive charge. At such…
Q: a) Draw all curved arrows that show the entire transformation of 1 into 6, and identify the entire…
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Q: Draw both resonance structures of the most stable carbocation intermediate in the reaction shown.…
A: Carbocations that are resonance stabilized as well as stabilized by hyperconjugation are more…
Q: The least Stable carbocation is
A: Given that : We have to identify the least stable carbocation out of the following :
Q: 2) Using one of the MO diagrams your developed in question 1, briefly explain the origins of the…
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Q: Complete the following acid-base reaction . Show all valence electrons on the interacting atoms and…
A: According to Lewis concept, an acid is an acceptor of electrons while a base is a substance that…
Q: Draw both resonance structures of the most stable carbocation intermediate in the reaction shown.
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Q: Which SN1 raction is faster in the given pair?
A: In the reaction it is said that reaction proceed by SN1 mechanism means there must be formation of…
Q: Which of the following represent a pair of resonance contributors?
A: By analyzing the given options we can find the given pair of resonance contributors.
Q: Draw a full orbital diagram for all the bonding and antibonding m orbitals in the three-membered…
A: It can be explained by huckel molecular orbital diagram.Now as it has three carbon atom participates…
Q: Which compound I or II is more basic? Justify your answer using orbital "cartoon" diagrams. CH3 CH3…
A: Compound one is more basic than two because lone pair of electrons on nitrogen atom is easily…
Q: Circle the most reactive molecule with water and put an X through the least reactive. CI
A: The molecules are acid derivatives:
Q: 2) For two of the following pairs of compounds, identify the most basic atom in each compound, and…
A: Here we have to find the most basic atom and the most basic compound from the given pair of…
Q: Draw arrows and all major and minor resonance contributors for the following molecules. Do not…
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Q: Which position(s) on the ring will be most likely to be sulfonated? Explain your reasoning for…
A: In the sulfonation Reaction, we can used sulfonating agent like SO3, py or SO3 / H2SO4. This reagent…
Q: 5. Follow the curved arrows and write the products. + BF3 a. b.
A: When two molecules interact, the molecule that has HOMO attracts the molecule with the LUMO. This…
Q: For the structure below a. Identify the longest conjugated system you can. b. Draw a resonance…
A: 1. We have to predict the longest conjugated system. 2.we have to draw resonance structure.
Q: Draw curved arrows that depict electron reorganization for the acid base reaction below. See below…
A: Please see explanation.
Q: 7. , Rank the following compounds in order from most electrophilic (1) to least electrophilic'.…
A: An electrophilic center is the one that seeks electrons (or negative charge).
Q: Draw the curved arrows and the resulting resonance structure of meta-nitrobenzoate that shows a…
A: Resonance structure: If the Lewis structure of a molecule or ion cannot explain by a single…
Q: Draw curved arrows to show how one resonance contributor leads to the next one.
A: a) Please find below the resonance contributors.
Q: Which is a resonance contributor for this molecule? :ö:
A: Resonance is delocalization of electrons.
Q: Complete the following acid-base reaction . Show all valence electrons on the interacting atoms and…
A: The acid base reaction is used to find the ph of the solution and it a chemical process that happens…
Q: Explain (using resonance forms and words ) why compound 1 undergoes hydrolysis faster than compound…
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Q: 2. Give the complete electron flow of the E2 reaction, be sure to clearly show the electrons that…
A: The answer to the given question is as follows------------ The problem in question 2 is an example…
Q: (Chapter 9) Write all of the resonance contributors for the following molecule. If the various…
A: The resonance structure of a compound is formed when the lone pair of electrons present on an atom…
Q: Construct MO energy diagrams for the cyclopropenyl cation, radical, and anion. Which of these…
A: The MO energy diagrams for the cyclopropenyl cation, radical, and anion are given below. (a) It…
Q: Use (2) curved arrows simultaneously to demonstrate resonance. Select the best possible contributor.
A: A multiple choice question based on resonance structure, which is to be accomplished.
Q: What is the base at offset 5 of GATTACA? Remember: the leftmost base has offset 0.
A: DNA is combination of two different kind of nitrogenous bases namely purine and pyrimidine and the…
Q: Could you explain why the highlighted group on the right side of the double bond has a higher…
A: Any substituent having higher atomic number takes more priority over a substituent with a lower…
Q: Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Long and detailed explanations…
A: When you mixed both in equal about then compound C not rotate plane polarized night because this…
Q: What carbons are electron deficient and the electron rich? Justify with all the correct resonance…
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Q: + CH3OH Draw curved arrows to show the proton transfer reaction between the aldehyde and the…
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Q: + CH3OH At least one atom does
A: Given Reactant 1. Acetaldehyde Reagent Base = Methoxide ion Product To be determined
Q: a. The reaction shown takes place in four steps. Complete the mechanism by adding curved arrows for…
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Q: In the box below each molecule write down the number of R-electrons. Circle all of the following…
A: Double bond = 1π bond Lone pair = 1π bond Only that lone pair is counted in π System which…
Q: 17. Which of the following violates the rules for curved arrows (when drawing resonance structures)?
A:
Q: How do I rank these from best to poorest leaving group? Do I base it in the size of the…
A: We have to rank leaving group tendency :-
Q: Define Protons on Benzene Rings ?
A: Benzene ring: It is organic hydrocarbon group having Carbon and Hydrogen as main elements in which…
Q: b) Support your answer with the appropriate energy diagrams. (Energy diagram should show two…
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Q: 0:z: :ö:
A:
Q: Use curved arrows and draw four additional resonance contributors. Please circle the most…
A: The ion given is,
Q: The unusual molecule below is aromatic and somewhat stable in spite of the positive charge on…
A: Note: Resonance is possible any double bond is conjugated with another double bond or atom is having…
Q: 4. Which do you think is more chemically stable, the reactants or products of each of the reactions…
A: As all the above process result in production of energy it means all reaction are exothermic.
Please explain which resonance contributor would be the best and why.
Step by step
Solved in 2 steps with 1 images
- 1)- add any nonbonding electrons 2)- Identification of the π system 3)- redraw σ system 4)- complete the resonance 5)- circle the best resonance contributionNeed help with Part 2: select all the appropriate resonance structures that result from the first step that is reproduced below.The drawing here on the right is the answer I submitted, but it says it is wrong and requires a carbocation.
- Use (2) curved arrows simultaneously to demonstrate resonance. Select the best possible contributor.NO2 would stabilize an adjacent (-) charge through resonance, making it a –R substituent What is the more acidic proton in nitrocyclohexane? explain with proper resonance structures of the conjugate base.Use curved arrows and draw four additional resonance contributors. Please circle the most significant contributor(s) to the resonance hybird and explain why.
- For each of the following groups of molecules (labeled A–E), rank the resonance forms in order from least important (5) to most important (1)Briefly explain why the I end of the molecule is more electrophilic than the Cl end.did I draw my final product correctly?how many dots should be there on oxygen in the final product?what formal charge should it be?
- For 1 and 2, use curved arrows to illustrate the potential overall electron movements or bond changes, and identify the type of reaction by examining the overall chemical transformation. Show A-H bonds as needed.Draw curved arrows to show the movement of the electrons as one resonance contributor is converted to the next.