Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of the compound below with base. H3C `N(CH3)2

Q: CH3 + NAOH CH CH CH CH A) II B)I C) II D) IV Which carbon atoms are most susceptible to nucleophilic…

A: Given, reaction is the acid-base reaction. Electron withdrawing groups like carbonyl group (CO)…

Q: a. H2C=CH2 b. (CHз)2С%3CH2 c. CH3CH=CHCH3

A: Increasing order of reactivity : a < c < b Reactivity of alkene towards hydrohalogenation is…

Q: Write reactions of propan-1-ol with the following reagents: a. Na b. PCl5

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Q: 3. Arrange the following in order of increasing reactivity towards a hydrogen halide. Explain. a.…

A: The order of increasing reactivity towards Hydrogen halide :

Q: ak the compounds in each group in order of increasing reactivity in electrophilic aromatic…

A: Note: According to our guidelines we are supposed to answer only one question.  Kindly repost other…

Q: Rank the following compounds from most reactive to least reactive in an electrophilic aromatic…

A: Electrophilic aromatic substitution: In an organic reaction in which an electrophile replaced an…

Q: Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the…

A: (a) The the major products of the reactions of naphthalene with HNO3, H2SO4 is predicted as follows,

Q: SCH3 OCH3 'Br `N(CH3)2

A: Given four compounds and asked to arrange them to their reactivity order.

Q: CH3 CH3 OEt NH3 A в D least reactive most reactive

A: Electrophilic aromatic substitution reaction takes place between the aromatic ring and electrophile…

Q: resonance and inductive effects if present.

A: Both phenol and benzene are nucleophilic in nature due to different reasons. Both, inductive and…

Q: Arrange the following compounds in order of decreasing acidity.CH3COOH CH3OH CH3CH3

A: The compounds given in the question are three different types of compounds based on the functional…

Q: O On a reaction with acid, 4-pyrone is protonated on the carbonyl-group oxygen to give a stable…

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Q: Rank the following monosubstituted aromatics from least to most reactive in electrophilic aromatic…

A: To solve this problem we have to consider the electron density in the benzene ring .  If there will…

Q: 4. Write out the steps necessary to convert the compound on the left into the compound on the right…

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Q: 2. p-Nitrophenol is not intensely yellow until it is deprotonated under the basic conditions of the…

A: p-nitrophenol undergoes deprotonation in basic condition to form p-nitrophenolate ion.

Q: Order the following phenols by their increasing acidity (least acidic first, most acidic last).…

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Q: Rank the phenols below in order of increasing of acidity ОН ОН ОН OH ОН а) b) c) d) e) NO2 CH3 ČI…

A: Acidity of any acid depends on the stability of the conjugate base formed after the removal of the…

Q: When one mol alkene treated with an acidic KMNO4 one mol 1,2 butanedione and two mole of CO2…

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Q: Draw the structure of A, an intermediate in the synthesis of the antipsychotic drug risperidone.…

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Q: Which of the following species is attacked by benzene in nitration reactions? O NO3* O NO2* O NO* O…

A: In an electrophilic aromatic substitution (EAS) reaction aromatic pi-bond attacks the electrophile…

Q: Draw the structure of the major organic product of the following reaction. =CH2 1. Hg(OAc)2, H2O 2.…

A: When Hg(OAc)2, H2O is treated with alken then 3 membered ring is formed as intermediate and then by…

Q: Arrange the following in order of increasing reactivity towards a hydrogen halide. Explain. a.…

A:

Q: What is the best way to accomplish the following transformation? ОН H. LNH2 HO, NH2

A: Look at the compound carefully , there are 3 groups present.  1) Keto group -CO- 2) amide group…

Q: 1. (a) Indene is considered much acidic compare to most hydrocarbons. It is readily reacting with…

A: A question based on introduction to organic chemistry that is to accomplished.

Q: 1. KOH NH2 N-H 2. H;NNH2 Alkyl halide

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Q: h resonance structures of the anion formed by the reaction of the most acidic C-H bond of the…

A: Acidity of hydrogen strength depends on the conjugate base formed when treated with base.The…

Q: methoxide ion. H- C H. formate ion methoxide ion Tahle HICIH エ

A: Given that The formate and methoxide ions are both formed by removing a hydrogen atom from a…

Q: 4. Give the major product of each of the HBr a. HC = CCH3 excess HBr b. HC = CCH3

A: The major products of the following reaction will be as follows:

Q: a Draw a structure for the neutral (uncharged) organic product of the reaction below. 1. NaH 2.…

A:

Q: Diphenhydramine, the antihistamine in Benadryl, can be prepared by the following two-step sequence.…

A: The structure of diphenhydramine has to be given.

Q: Identify the nucleophile and electrophile in the following acid-base reaction of acetone I and…

A: Electrophile means electron loving group and nucleophilic means nucleus loving group.

Q: Which nitrogen in the aromatic compound below is least basic? (3) (1) HN EN A B OC O -NH₂ (2)

A: Well, as we know in order to find the Basicity we need to see how easily the the particular atom can…

Q: Which of the following compounds would undergo a diazotization reaction? - 1. NH2 2. 3. CH;CH;NH -…

A: Option 2 is Correct Answer. It means only aniline undergo diazotization.

Q: Diphenhydramine, the antihistamine in Benadryl, can be prepared by the following two-step sequence.…

A: The 1st step of the reaction involves a hydride reagent NaHreducing agentThe second step involves…

Q: Which of the following phenols would have the largest pKa? но O2N HO. HO. I II III OH IV О а. | O b.…

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Q: Which of the following has the MOST acidic hydrogen? Select one: a. 3-hexanone b. 2,4-hexanedione c.…

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Q: 2. Draw the structure of the product for each reaction: a. OH K,Cr,0, H+ b. OH Conc. H,SO4, 180°C…

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Q: Draw a structural formula for the substitution product of the reaction shown below. H CH3 NH3 CH3OH

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Rank the reactivity of the compounds below toward nucleophilic acyl substitution by writing the…

A: Interpretation: We have to arrange the given molecule in the order of their nucleophilic…

Q: When enamine A is reacted with methylbromide (CH3-Br) two products B and C can form. Br B H3C-Br CH3…

A: Enamine gives nucleophilic substitution reactions with alkyl halides.

Q: B) Write the most stable enol forms of the following compound, and choose which of them is more stal…

A: In this question, we will write down the most stable enol form for the given compound and also we…

Q: Which one of the following compounds give racemic mixture when treated with NaOH (aq)? A…

A: To obtain racemic mixture we know that the reaction should proceed through SN1 reaction mechanism.…

Q: Which carbon of indole is easily attacked by an electrophile? 4 5, 2 A. 2 В. 3 С. 4 D. 5 ZI

A:

Q: Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of…

A: The acidic hydrogen will be the hydrogen of the compound which can be removed easily, or in other…

Q: 4. In the following compound: (a). Circle the good leaving group. (b). Explain why it is a good…

A: The good leaving group is that in which the negative charge is stablised.

Q: Which of the following bases would quantitatively convert 1-butanol into sodium 1-butoxide? NaH NAOH…

A: Any base which is can react with alcohol to produce less acidic and basic compounds will only…

Q: Draw the structure of the major organic product of the following reaction. CH3 1. Hg(OAc)2, H2O 2.…

A: This is an example of oxymercuration-demercuration reaction in which greater substituted alcohol is…

Aldehydes and Ketones

Aldehydes and ketones are organic compounds that have a carbonyl group, C = O, as their functional group. They both differ in the placement of this carbonyl group in their structures.