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…
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Q: Draw both resonance structures of the most stable carbocation intermediate in the reaction shown.…
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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…
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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…
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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…
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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.
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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)?
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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:
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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.
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- b) Draw the most important (most stable) resonance structures for the compound below. With the help of the resonance structures, explain which of the two nitrogen atoms is more basic.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.Current Attempt in Progress For the given cation, draw all significant resonance forms and rank them from most significant to least significant. Briefly explain the rankings. Part 1 Ⓒ H Because this is a charged species, let's focus on resonance patterns that can delocalize the charge. First, add curved arrow(s) to show the resonance using the following pattern: a lone pair next to a carbocation. Modify the second structure given to draw the new resonance structure. Include relevant formal charges in your structure. Use the + and tools to add/remove charges to an atom, and use the single bond tool to add/remove double bonds. Part 2 Edit Drawing eTextbook and Media Save for Later Attempts: 0 of 3 used Submit Answer
- All resonance structures with arrow. Major resonance?x-xo B Draw molecule A. On that drawing include the lone pairs and the curved arrows that would produce resonance structure B.Curved arrows are used to illustrate the flow of electrons. Using the provided resonance structures, draw the curved electron- pushing arrows to show the interconversion between resonance hybrid contributors. Be sure to account for all bond- breaking and bond-making steps. I I I I :O: f
- If possible, draw additional resonance contributors for the structure below. Include appropriate curved arrows showing how one contributor is converted to the next. If you believe there is a major resonance structure, circle it. (Hint: You should start by filling in lone pairs of electrons that have not been depicted. And you may find it useful to draw in implicit Hs.)..1. Draw ethylbenzene and put a + on the carbon next to the benzene (innermost carbon in ethyl group). Show all resonance forms for this ion. 2. draw the naphthalene and put one - on the neighboring carbon of the "crossroads". show every resonance forms for this ion. 3. Draw benzoic acid and draw on all p-orbitals.Which arrow (x, y, or z) points toward the most acidic proton in the molecule to the right? (Arrows pointing toward C can be assumed to point at the H attached to that C.) Which structural feature plays the most significant role in influencing the relative acidities of the indicated protons? a. inductive effect b. size c. resonance d. hybridization
- H Select to Add Arrows H H H H H Li Ⓒ Li Ⓒ Problem 3 of 21 Please select a drawing or reagent frBe sure to answer all parts. The pk of three different C-H bonds is given below. For each compound, draw the conjugate base, including all possible resonance structures for compound C. Use skeletal structures when drawing all conjugate bases. compound A H H H pK₂ = 50 Conjugate base of compound A: Conjugate base of compound B: Conjugate base of compound C: edit structure ... compound B resonance structure (negative charge on C) H H edit structure ... (one Lewis structure) edit structure ... (one resonance structure) X H pka = 43 compound C edit structure ... H H pK₂ = 19.2 resonance structure (negative charge on O) H5. Draw all resonance structures for the following molecules and indicate the minor and major contributors.