1. Explain the the following,giving examples and illustrations to support your answer Electrophilic aromatic substitution reaction: Iodination
Q: Prove the aromaticity of the molecules given below by discussing them.
A: Since you are posted with multiple sub-parts. As per the rule I am answering the first three…
Q: Aromaticity On the basis of Huckel's rule, label the following molecules as aromatic, nonaromatic or…
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Q: Rank these nucleophiles from most to least reactive for substitution reactions and give a brief…
A: The nucleophilicity of a species depends on various factors such as negative charge density,…
Q: Provide a short paragraph that relates the most essential elements of theory (reactivity,…
A: Electrophilic Aromatic Substitution Reaction is described below:
Q: Complete the missing structures in the Cannizzaro reaction below. кон aq phase organic phase H*
A: The question is based on the concept of organic Reaction. we have been given cannizzaro reaction. We…
Q: Why methyl benzoate is mainly meta orienting? Explain it with the help of charge formation in the…
A: We have to show with help of charges why the methyl benzoate is meta director not ortho/para…
Q: which is more basic?? pipyridine or pyridine Explain with resonating structure?
A: According to Lewis definition of acid and base, a base is a substance that can donate a pair of…
Q: 1) How will you describe whether any compound has been oxidized or reduced? Support the answer with…
A: Hi, we are supposed to answer one question. To get the remaining questions solved please mention the…
Q: = Study and classify the following reactions as S (substitution), E (elimination) or ■). Explain…
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Q: (b) The following compound (2) is a natuml product drug. Using the criteria for aromaticity and your…
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Q: (a) Illustrate the following name reactions by giving example :(i) Cannizzaro’s reaction(ii)…
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Q: ring with the effect of ……………… and are ……………………… directed towards electrophiles. Groups that are…
A: If any group increases electron density on benzene is ortho para directing. If it withdraw electron…
Q: Although chlorine is an electron withdrawing group, yet it is ortho-, para¬directing in…
A: The function of an electron-withdrawing group withdraws the electron from the ring of the compound.…
Q: Compare isoquinoline and quinoline..Explain their basicity.Which of them will be more susceptible to…
A: Isoquinoline and quinoline are heteronuclear organic compound with one aromatic phenyl group and one…
Q: (a) Discuss the aromaticity of a six membered heterocyclic compound which is weak base in nature.
A: A question based on aromaticity that is to be accomplished.
Q: Outline the synthesis of 2-pentyne from acetylene and any other needed organic or inorganic
A: The reaction scheme is generally framed by considering the factors like atom availability and…
Q: following in the order of the Arrange reactivity to electrophilec aromatic Substitetrion reaction…
A: Since you have asked multiple questions, we will solve the first question for you. If you want any…
Q: Rank imidazole, pyrrole, and benzene from most reactive to least reactive toward electrophilic…
A: Electrophilic substitution reaction- The replacement one atom or group of atom from reactant species…
Q: Which of the statements below is true regarding the reactivity of benzene? a. Substitution is…
A: Given, Which of the statements below is true regarding the reactivity of benzene? Options are :…
Q: When attempting to synthesize an alkyne, why is the hydrogen on the right abstracted instead of the…
A: This can be explained as:
Q: Benzene Colto, ) was found to be totally unroactive toward addition Reactions. Based upon Resonance…
A: Here we have to explain why addition reaction of benzene is completely unreactive according to…
Q: p-Fluoronitrobenzene is more reactive toward hydroxide ion than is p-chloronitrobenzene. What does…
A: The hydroxyl ion attacks the carbon having the leaving group from a trajectory that is nearly…
Q: aminophylline is a good water soluble derivative of theophylline as ethylene diamine derivative in…
A: Aminophylline is a ethylene diamine derivative of theophylline and it is water soluble. Presence of…
Q: fill in the blanks. If there are unshared pairs of electrons on the atoms directly attached to the…
A: Explanation- 1) Electron donating groups cause the second subtituent to add on to the para or ortho…
Q: 1. Explain the the following,giving examples and illustrations to support your answer Electrophilic…
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Q: Which organic compound will yield the following result: methylamine, octanoic acid, or octanylamine?…
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Q: 1. Is the following compound aromatic or not? Motivate your answer by using Huckel's rule."
A: Since you have asked multiple questions, we will answer only first question for you. In order to get…
Q: group exists in benzene ring. a) Give two (2) examples of meta director substituents. b) Predict the…
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Q: Without reading ahead in L Chapter 20, state whether it should be possible to carry out each of the…
A: The reactivity of the acid derivative depends on the partial positive charge on the carbonyl carbon…
Q: what is the Mechanism and important examples of aromatic Nucleophilic Substitution reactions
A: The substitution reaction which take place on an aromatic ring via nucleophile.
Q: Define Inscribed Polygon Method for Predicting Aromaticity ?
A: To predict whether a compound has π electrons completely filling bonding MOs, we must know how many…
Q: 1) Which one more reactive to word nucleophilic substitution P- nitro toluene or O- ethyl toluene ?…
A: P-nitro toulene will be more reactive towards nucleophilic substitution than O-ethyl toulene because…
Q: a) b)
A: Aromatic compounds are those compounds which follow huckle's rule that is the compound should have…
Q: With diagrams and detailed explanations, comment on the electrophilic aromatic substitution…
A: Quinoline and isoquinoline are the hetrobicyclic compounds. Both quinoline and isoquinoline undergo…
Q: Question 9 Why is the compound shown NOT considered aromatic?
A: A ring-shaped cyclic molecule is said to obey the aromaticity if it obey huckel rule. Huckel rule…
Q: Draw the resonance structure of the following compounds and identify if aromatic or nonaromatic In…
A: Huckel's rule suggests us the structure as aromatic , non aromatic and antiaromatic. The rule is as…
Q: Provide the name of the functional group attached to the aromatic ring. "Do not include aromatic in…
A: We are given an aromatic compound with functional group.
Q: Solve the attached
A: Resonating structure of acetic acid is Resonating structure of ethyl acetate is Resonating…
Q: Provide mechanism (arrow pushing) for this Friedel Crafts alkylation, include electrophile and…
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Q: By which substitution mechanism (SN1 or SN2) did the reaction occur? How did you know? For what…
A: The reaction is happened via SN1 mechanism. In SN1 mechanism first leaving group leaves in rate…
Q: Question 7 Nation Ntion is an example of elecphc aomatic sb on Indicate the uclephile and electrophe…
A: The substitution reaction of an aromatic compound by a nitronium electrophile is called nitration…
Q: To what do you attribute the deactivating nature of halides in electrophilic aromatic substitution?…
A: Halogens are deactivating groups which decreases the rate of electrophilic aromatic substitution.…
Q: b. Predict the product of the reaction between the enamine from part a and ethyl iodide. Hint:…
A: In this question we have to tell the product of the reaction.
Q: 7. Outline a synthesis for each of the following alkynes, using any necessary organic or inorganic…
A: Given reactions:
Q: answer....given below some compounds give the rank most reactive to least reactive in an…
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Q: electrophilic aromatic displacement reaction by drawing the structures of the compounds given below…
A: Aromatic Electrophilic substitution reactions:
Q: Please give a clear handwritten answer of this structure classified in aromatic and…
A: Given; structure of molecules
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- Although chlorine is an electron withdrawing group, yet it is ortho-, para¬directing in electrophilic aromatic substitution reactions. Explain why it is SO?Give a clear handwritten answer...complete the following reactions with detailed explanation neededWhy methyl benzoate is mainly meta orienting? Explain it with the help of charge formation in the benzene ring ( ortho, meta and para position) Show Structures in methylbenzoate.
- With diagrams and detailed explanations, comment on the electrophilic aromatic substitution reactivity of quinoline and isoquinoline(a) Illustrate the following name reactions by giving example :(i) Cannizzaro’s reaction(ii) Clemmensen reduction(b) An organic compound A contains 69.77% carbon, 11.63% hydrogen and rest oxygen. The molecular mass of the compound is 86. It does not reduce Tollen’s reagent but forms an addition compound with sodium hydrogen sulphite and gives positive iodoform test. On vigorous oxidation it gives ethanoic and propanoic acids. Derive the possible structure of compound A.Give a clear explanation handwritten answer....given below some compounds give the rank most reactive to least reactive in an electrophilic aromatic substitution reaction
- Provide a short paragraph that relates the most essential elements of theory (reactivity, regiochemistry and rate etc) behind the EAS reaction. (Electrophilic Aromatic Substitution Reactions)Give a clear handwritten answer....complete the following reaction....What is the background on the chemistry of electrophilic aromatic substitution reactions, what is the importance of nitration reactions in organic synthesis, and the reactivity of methyl benzoate, a methyl ester of benzoic acid. With references
- Give a clear handwritten answer with explanation..Complete the following reactions?Rank these nucleophiles from most to least reactive for substitution reactions and give a brief rationale for your answer.Preferably in a flowchart, what is the Mechanism and important examples of aromatic Nucleophilic Substitution reactions