[References]Classify the following substituents according to whether they are electron donors or electron acceptors relative to hydrogen bythe resonance and the inductive mechanisms.a = acceptord = donorn = no effectö:Inductive effectResonance effect:0:1. --CH2CH2CH2-N+:0:2.3.-C-CH2CH2OH:0:11+-S-CH3CH3Inductive effectResonance effectInductive effectResonance effectSubmit AnswerRetry Entire Group3 more group attempts remainingF3F4►II4$RCengage Learning Cengage Technical SupportPrtScnHomeEndPgUpF5F6F7F8F9F10< 6%25Λ&729()890TYU

Resonance Effect:The resonance effect refers to the delocalization of electrons through π bonds or…

Answered: [References] Classify the following…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 19E

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Which of these products is the result of a hydride shift occuring during the substitution reaction of aqueous 2-chloro-3-methylpentane? CH3CH2CCH2CH3 || CH2 CH3CH(OH)CH(CH3)CH2CH3 CH2=CHC(CH3)=CHCH3 CH3CH=C(CH3)CH2CH3 CH3CH2C(CH3)CH2CH3 | OH
Classify your he following substituents according to whether they are electron donors or electron accepters relative to hydrogen by the resonance and the inductive mechanisms a= acceptor D=donor n= no effect please double check and see everything is correct I had submitted this question multiple times and gotten it incorrect I have no more ask questions left to send.
Below is a mechanism that represents the following single reaction sequence: a certain alcohol undergoes acid- catalyzed dehydration (conversion that involves the loss of water from the reacting molecule or ion) to form an alkene product. Write the IUPAC name of the product. Include E/Z stereochemistry. Hint: Name of the substituent of the product is similar to that of reactant. * :ÖH :O: :0: :O: 1-phenylpropanol oxonium ion H. нон Carbocation stabilised by resonance loss of water benzylic carbocation organic product + H-B Alkene formed ;B proton abstraction
which letter shows the major product
Bromine is a larger atom than chlorine, but the equilibrium constants in Table indicate that a chloro substituent has a greater preference for theequatorial position than does a bromo substituent. Suggest an explanation for this fact.
answer it properly
Which of the following rings is the most strained? cyclopropene; cyclopropane; cyclobutane; cyclopentane; cyclohexane after finding the most strained compound explain why and compare it to the other answer choices, explaining why they do not work as an answer.
> acetone > ethane - Two molecular ions H3C-CH₂-CH₂-COR and have undergone McLafferty rearrangement and Ortho effect respectively. What are the possible fragments obtained as a result of these processes ? COOCH3 OH + -COH]: [CH₂O and Co] CO (A) (B) x] : [GH₂C (C) RH, C₂H₂ and CH₂CO: [(CH₂O), CO and CH₂OH] (D) H₂CCROH and C₂H4; [(CH₂O), CO and CH₂OH] R-CH₂-CH₂ - CH₂ - COH H₂C=CR = CROH and H₂C = CH₂ C₂H403 and CH4 P.T.O.
dont provide AI solution....
Explain why the halo-substituted benzenes have the relative reactivities
Provide the systematic name for each of the following isomeric esters with the chemical formula C₂H1202. (Be sure to indicate double bond stereochemistry using (E)/(Z) notation. Indicate stereochemistry in rings with the terms cis or trans. It is not necessary to use italics in writing compound names.) ball & stick ✓- + labels (E)-methyl 3-methylpent-3-enoate An error has been detected in your answer. Check for typos, miscalculations etc. before submitting your answer. ball & stick + labels isopropyl-2-methylacrylate ball & stick - + labels (E)-ethyl pent-2-enoate 12
Can someone help me solving this reaction? :)

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