Q: (i) Write Reimer-Timann reaction.
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Q: How can you tell a substituent will donate negative charge into an aromatic ring? A) There is an…
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Q: Use the inscribed polygon method to show why cyclobutadiene is not aromatic. cyclobutadiene 4 x…
A: To find: Show why cyclobutadiene is not aromatic using inscribed polygon method
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A: Aromaticity is a property of conjugated cyclic systems in which the stabilization of the molecule is…
Q: Which (if any) lone pairs are participating in aromaticity?
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Q: why is cyclopentadiene more acidic than cycloheptatriene?
A: cyclopentadiene more acidic than cycloheptatriene it can be explained by aromaticity
Q: Explain how heteroduplex formation is resolved during transformation?
A: We have find out heteroduplex formation is resolved during transformation.
Q: НО :0:
A: Rp
Q: styrene as shown in the box? H R• + ? нн H R н-с-с- R-C-с. А) B) нн нн H R R-ċ-C нн C) D) нн I-U O-I
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Q: Would [16]-, [20]- or [22]-annulene be aromatic if each ring is planar?
A: The aromatic nature of [16]-annulene, [20]-annulene and [22]-annulene has to be predicted.
Q: How is this aromatic
A: Generally aromaticity of molecule is predicted by Huckel's rule.
Q: Classify the diene as conjugated, isolated, or cumulated: Classify the diene: conjugated isolated…
A: Answer: the given diene is a conjugated diene so option A is correct
Q: Would [12]-, [22]-, or [36]-annulene be aromatic if each ring is planar?
A:
Q: Would [16]-, [20]-, or [22]-annulene be aromatic if each ring is planar?
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Q: 5Thiamin, or vitamin B1, contains a positively charged five-membered nitrogen–sulfur heterocycle…
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Q: Give two examples each of Unsymmetrical alkenes and reagents and give two examples of reactions of…
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Q: Are terminal alkynes considered weak or strong acids? Explain why.
A: Welcome to bartleby ! Introduction : We have to tell terminal alkynes are weak or strong acids .
Q: Organic chemistry:What is Grignard reagent /synthesis used for ? And how can you tell if a a…
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Q: 2. State the two main experiments that were used to establish the extra stability of the benzene…
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Q: The Diels–Alder reaction, a powerful reaction discussed in Chapter 14, occurs when a 1,3-diene such…
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Q: Explain the Stability of Allylic Carbocations ?
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Q: Define Electrophilic Aromatic Substitution ?
A:
Q: Is this molecule aromatic, antiaromatic, or nonaromatic? aromatic nonaromatic antiaromatic
A: A molecule that is neither aromatic or antiaromatic. Aromatic molecules are cyclic, conjugated,…
Q: Draw the molecules from their IUPACn 5-ethoxy-5-fluorooct-3-yne
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Q: Use the Hammond postulate to explain why (CH3)2C = CH2 reacts faster than CH3CH = CH2 in…
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Q: which of the structures is aromatic, according to Huckle? list the 3 features that make them…
A:
Q: N-
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Q: Explain the General Features of Radical Reactions ?
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Q: Which structure Is aromatic and has six electrons In the conjugated system? Click on a letter A…
A: Aromatic compound which follows huckel's rule i.e. 4n+2 rule where n is natural number.
Q: What are Allylic Carbocations ?
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Q: Select the single best answer. Would [32]−, [16]−, or [22]−annulene be aromatic if each ring is…
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Q: Which of the structures shown below is not aromatic? Click on a letter A to D to answer. CH, CH, B D
A: Aromaticity of a compound is defined as a property of delocalization of pi electrons which enhances…
Q: Why is 5-octene not possible? 2. Why is 3,3-dimethyl-3-octene not possible?
A:
Q: A. Determine the number of electrons in a system of cyclic conjugation (zero if no cyclic…
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Q: Show the procedure for Naming Aromatic Rings as Substituents ?
A: Aromatic rings are used as substituents if some higher priority groups are resent in the molecule.
Q: why a CH3 group directs electrophilic aromatic substitution to theortho and para positions ?
A:
Q: Draw the structure of cyclobutane. Select Draw Rings More
A: Cyclobutane is a cycloalkane and organic compound with the formula (CH2)4
Q: What is Williamson ether synthesis ?
A: Given reaction name, Williamson ether synthesis
Q: Explain the Rule of Endo Addition ?
A: The rule of endo addition has to be explained below.
Q: Define features of nucleophilic addition ?
A: There are different types of organic reactions – Substitution reaction Addition reaction
Answer part C
Aromaticity is a characteristic in which any planar system in which there is complete delocalisation of pi electron in the ring,and the system contain 4n+2 pi electrons in the ring is called aromatic.
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- Which of these images are not aromatic?Using the Frost Circle method to outline the molecular orbitals of cyclobutadiene. and identify whether it is aromatic, antiaromatic or non-aromatic. Explain. (Note: Show the outline of MO of cyclobutadiene using the Frost circle method)Use the inscribed polygon method to show the pattern of molecularorbitals in cyclooctatetraene.Classify the dianion of cyclooctatetraene as aromatic, antiaromatic, ornot aromatic, and explain why this is so.
- Use the inscribed polygon method to show the pattern of molecularorbitals in cyclooctatetraene. Classify the dianion of cyclooctatetraene as aromatic, antiaromatic, ornot aromatic, and explain why this is so.Are the following molecules aromatic, antiaromatic, or non-aromatic? Why?Label the following molecules as aromatic, anti-aromatic, or non-aromatic. For the ones that aren’t aromatic, explain why they are either non-aromatic or anti-aromatic.
- Predict whether the cyclic system is aromatic , anti-aromatic, or non-aromatic by counting electrons and explain why ? Also circle all the basic nitrogen’s wherever possible . Show all lone pairs which are involved in cyclic delocalization?what aromatic annulene has the same number of bond molecular orbital as the hypothetical all cis (20) annuleneAdd electrons to your energy diagram to show the configuration of the cyclopropenylcation and the cyclopropenyl anion. Which is aromatic and which is antiaromatic?
- Explain how to construct the molecular orbitals of a conjugated cyclic system similar tobenzene and cyclobutadiene. Use the polygon rule to draw the energy diagram, and fillin the electrons to show whether a given compound or ion is aromatic or antiaromatic.Use the inscribed polygon method to show the pattern of molecularorbitals in cyclooctatetraene. Indicate the arrangement of electrons in these orbitals forcyclooctatetraene, and explain why cyclooctatetraene is not aromatic.Using the rules of aromacy determine if the following compounds A,B,C are aromatic and explain why