A. -Br D. 0-CH3 E. acats Rank in arder of increasing reactivity towards electrophilic aromatic Subsitution. C. B.

Q: Draw the products of the following reactions, including all stereoisomers:

A: Given reactions,

Q: Synthesize a Sudan I. What method should be used and why?

A: It is prepared by diazotization of anthranilic acid followed by coupling reaction with…

Q: H H

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Q: 2. Write "most" under the compound which is most reactive toward electrophilic aromatic substitution…

A: “Since you have asked multiple question, we will solve the first question for you. If you want any…

Q: e starting materials and reaction conditions suitable for lowing compounds by a procedure involving…

A: As per guidelines first 3 are allowed to answer , please post seperately rest of the subparts to…

Q: a) Which is more reactive towards Electrophilic aromatic substitution (EAS)? (b) Which of the…

A: Note: according to our guidelines we are supposed to answer only first three subparts. Kindly repost…

Q: What diene and dienophile are needed to prepare attached compound by aDiels–Alder reaction?

A: Diels Alder reaction is an essential organic reaction. It involves the conjugate addition of diene…

Q: 5. Provide the missing reagent indicated by "???": Br ???

A: “Since you have asked multiple question, we will solve the first question for you. If you want any…

Q: Explain why methyl vinyl ether (CH2 = CHOCH3) is not a reactive dienophile in the Diels–Alder…

A: Diels-alder reaction is a cycloaddition reaction in which two molecules combine to form a new ring.…

Q: Vhich is the better nucleophile in protic solvent? or O CI-

A: Solvent which gives hydrogen ions in solution called as polar protic solvent whereas solvent which…

Q: Explain Radical Halogenation at an Allylic Carbon ?

A: An allylic carbon is a carbon atom bonded to a carbon atom that is bonded to another carbon atom.

Q: Why Aniline point adopted a rough measure of the content aromatic ?

A: Since you've posted multiple questions, we'll solve only the first question for you. if you want any…

Q: Which carbon will be the best site for electrophilic aromatic substitution? A C

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Q: AICI heat D raw a suitable resonance struetue (aronatic) is following annulene aromatic or not ?…

A:

Q: c. Please rank the following radicals in order from least to most SELECTIVE: A В C D Please explain…

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Q: a. Rank the follow radicals from least to most stable. CH3 CH3 CH3 .F A B C D Now, explain…

A: Radical is a electron deficient species. Any electron donating group stabilize it and electron…

Q: B A OH Compound A can be converted to cyclobutanol using the reagent Compound B can be converted to…

A: Organic chemistry in which we deal with organic reactions which covert organic reactant in to…

Q: Draw the products of the attached Diels–Alder reactions. Indicatestereochemistry where appropriate.

A: To find the product of the below Diels-Alder reaction

Q: The bicyclic heterocycles quinoline and indole undergo electrophilic aromatic substitution to give…

A: (a) Here, the substitution does not occur on the ring which has a nitrogen atom since the lone pair…

Q: Arrange the compounds in  set in order of decreasing reactivity (fastest to slowest) toward…

A: Electrophilic substitution is the substitution of H of an aromatic ring by an electrophile. The…

Q: ) Show full rxns/mechanisms with major product/s Aniline with SO3 in H₂SO4 catalyst Benzoic acid…

A: Aniline with SO3 in H₂SO4 catalyst Benzoic acid with Br₂ and FeBr3 catalyst Nitrobenzene with…

Q: Explain Retro Diels–Alder Reaction ?

A: To study the Retro Diels -alder reaction

Q: Rank the following dienophiles in order of increasing reactivity.

A:

Q: The indicated lone pair participates in aromaticity. H. O True False

A: "N of NH is sp2 hybridized and its lone pair of electron takes part in conjugation."

Q: HBr can be added to an alkene in the presence of peroxides (ROOR). What function does the peroxide…

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A: Given compounds,

Q: Consider the tetracyclic compound with rings labeled A–D. (a) Which ring is the most reactive in…

A: Benzene ring is activated towards electrophilic substitution reaction if there is an electron…

Q: Resveratrol is an antioxidant found in the skin of red grapes. Its anticancer, anti-inflammatory,…

A: Given compound,

Q: f. SN1 SN2 E1 E2 CH3CH2CH2BR + CH3O Product(s) of reaction f

A: In this question, first we select the correct type of Mechanism and then give the Product of the…

Q: What diene and dienophiles are used to make the following compounds? b. :a.

A: Answer:- This question is answered by using the simple concept of Diels -Alder reaction in which…

Q: Provide a synthetic route to the following compound(s) а. Br он from "H b. from SCH3

A: a) Since the configuration of carbon is changing in the product. Hence it means the conversion of…

Q: And Allyl / Phenyl compound are most reactive towards SN2 because of resonance stabilization. then…

A: SN^2 reaction is a single step process. SN^1 reaction is a two step process. SN^1 reaction involves…

Q: Arrange the compounds in  set in order of decreasing reactivity (fastest to slowest) toward…

A: Given compounds,

Q: H;C CH3 HN- -c-CH, A в a) Which of the above molecules (A or B) have a higher rate of reaction…

A: We have two compounds, we have to predict the rate of electrophilic aromatic substitution of the…

Q: What diene and dienophile are needed to prepare attached product ?

A: This is a diel's alder reaction in which a diene reacts with a dienophile to give the desired…

Q: Which of the following statements best describes why I- is a better nucleophile than F in solution?…

A: e is correct answer. A and B both offer explanations as to why I- is a better nucleophile than F- in…

Q: reagents x and y are?

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Q: Rank the four arometic rings below by reactivity (least reactive to most reactive) when mixed with…

A:

Q: Which substituent activates a benzene ring the most for electrophilic aromatic substitution? -F - Me…

A: The Electron donating substituents are electron rich groups which activates the benzene ring for an…

Q: Provide the whole reaction mechanisum teneration of electrophile, nudeophile bond formation, bond…

A:

Q: 4) Pick which one of the conjugated dienes would be preferred for 1,2-/1,4-additions as well as…

A:

Q: Which of the following is not aromatic? a. b. +, с. d. All are aromatic O b a Z. Z-H

A: That ring is not aromatic which not follow 4n+2 rule. Where n is number of electrons. Remember :- n…

Q: b) Explain why m-xylene undergoes nitration 100 times faster than p-xylene.

A: In nitration, NO2+ is the electrophile. Methyl group activates the benzene ring towards…

Q: How can pentan-2-one be converted to each compound?

A: Formation of the compound a from pentan-2-one is; Formation of the compound b from pentan-2-one is;…

Q: Azulene, an isomer of naphthalene, having fused 5 and 7 membered rings, has the following orbital…

A: Azulene: It is non-benzenoid fused ring system in which 5-membered and 7-membered ring systems are…

Q: Explain, with reference to the mechanism, why addition of one equivalent of HCl to diene A forms…

A: The given reaction is, Here, conjugated dienes undergo electrophilic addition to gives a mixture of…

Q: Explain why the halogens, when attached to a benzene ring, weakly deactivate the ring toward…

A: Halogens bonded to benzene ring has three lone pairs. These three electron pairs can cause resonance…

Q: (a) A compound known to be a substituted cyclohexanone derivative has lamda max of 235 nm. Could…

A: a) It is said that the compound is a substituted cyclohexanone.   This means the compound is a…

Q: Rank the nucleophiles in each group in order of increasing nucleophilicity.a. -OH, -NH2, H2Ob. -OH,…

A: Nucleophilicity increases with increase in basicity of species.  Across a period from right to left…

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.