Drag and drop the appropriate reaction conditions over each arrow as appropriate. Keep in mind the differences between acidic and basic conditions in the ring-opening of epoxides. OH ÓMe A OMe OH OH NM22 ŅM22 OH NaOMe MeOH H2SO4 MeOH NaNMe2 HNME2 H2SO4 HNME2

Q: draw the electrophilic aromatic substitution (EAS) mechanism for the reaction with +NO2, water…

A: Electrophilic substitution of benzene derivatives: In electrophilic substitution of benzene, one of…

Q: Here in Chapter 23, we learned that aniline becomes highly deactivated in the presence of a strong…

A: Given: Aniline is highly deactivated in the presence of a strong Lewis acid, due to coordination of…

Q: OEt Drag the appropriate labels to their respective targets. Rese H H H. NaOEt NAOH Ph Ph OEt EtO…

A:

Q: In synthesis shown in box, which of the following reagents is expected to give the indicated pro 1.…

A: Esters can undergo hydride reduction with LiAlH4 to form alcohol.

Q: BOH)2 Pd(PPH3)4 Br K2CO3

A:

Q: Please provide a way to synthesize the target compound using the reagents given below once Target…

A: The conversion reaction is given in the following step.

Q: Retrosynthesis for: OH Br product starting material

A: Retrosynthetic Analysis or Retrosynthesis is a planned approach for organic synthesis reactions. The…

Q: Complete the mechanism for the reaction of butanone with NABH, followed by the addition of aqueous…

A: When a ketone is reduced with sodium borohydride and acidic hydrolysis, then ketone is changed into…

Q: CH3 N. CH3 Но Ph

A: For retrosynthetic analysis one has to identify the compound, should have the knowledge of…

Q: Br SO3H T T T Arial

A:

Q: Chemistry Help woth this three retrosynthesis. thank you Provide a retrosynthesis and a forward…

A: TM 1 : Epoxide opened with 1-napthol. TM 2 : see below. TM 3 : Ethyl benzoate is subjected to Fridel…

Q: explanation

A:

Q: The compound below can react rapidly via an Sn1 process: OTs Select the explanation of why this…

A: Answer is explained below.

Q: OH (TM) (CH₂)4CH3 (SM) H

A: Here we have to synthesize the following given target compound from the given starting material by…

Q: alkenes possessing five carbons or fewer. OEt ethyl acetoacetate or EtO OEt diethyl malonate and…

A:

Q: 6 Show how to synthetize the following target: (a)

A: Organic reaction mechanisms.

Q: Perform retrosynthetic analysis for the following target molecules and show how TO torward synthesis…

A: It is a technique used for solving complex molecules. The target molecule is transformed into…

Q: For each pair of aromatic compounds, determine which will undergo electrophilic aromatic…

A: Since your question has multiple sub-parts, we will solve first three sub-parts for you. If you want…

Q: In this reaction, which species acts as the electrophile? Click on a letter A through D to answer.…

A: The species which act as an electrophile are the ones that are electron deficient. The species…

Q: e. Hint: heat is necessary to generate carbocations AND the concentrated acid conditions minimize…

A: Given reaction is the elimination reaction. In the elimination reaction, protonation of alcohol…

Q: A student attempted to synthesize an epoxide according to the reaction scheme shown here, but no…

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Q: a) DCI

A: Deuterium chloride is a strong acid. In the presence of strong acid, benzene can be protonated to…

Q: HO HO но SH

A: Nucleophilicity is an ability of the particular nucleophile to attack on the electrophilic center.

Q: How will the reaction rate of the SN1 roaction change if the alectrophile is switched from the…

A:

Q: 8. a) Propose a mechanism for the following electrophilic aromatic substitution reaction used to…

A: Given

Q: Show how the following synthesis could be carried out. More than one step is required. он „CN (+…

A: We will write the conversion

Q: CO₂E1 i CH3CHCO₂E 1. Na* "Ot 2. PhBr 3. H30, heat The intended reaction is the because the alkyl…

A:

Q: of KOH / CH;OH HO,

A: Organic reaction mechanisms:

Q: Propose a mechanism for each of the following reaction. (i) CH2-SMe2 Ph3 B PHCH2OH (ii) H2O2/ NaOH

A: The given reaction is, The mechanism for the reaction is shown below,

Q: Show the synthesis for the following Reactions. M Ô olt Nit2 Br -NH₂

A: Please find the attachment

Q: 1. BH3 THF 2. H₂O2/NaOH/H₂O ●

A:

Q: Which observation is NOT consistent with an SN1 mechanism for the conversion of an alcohol Into an…

A: a) In SN1 reactions, the intermediate formed is carbocation. When alcohols reacts with HX (where HX…

Q: Drag the appropriate items to their respective bins. CH3 CH= CH2 CH3 CH3CH(CH3)CH,NH2 CH3CH2COO…

A: Attacking reagents can be classified into two types  Electrophiles (E+)  Nucleophiles (Nu-)…

Q: NH,NH2 of `NHNH2 pyridine H20 -ОН HO

A: The first reaction given is the reaction of acid chloride with hydrazine and the second reaction…

Q: Explain why the following reaction yields the Hofmann product exclusively (no Zaitsev product at…

A: Given reaction  This is an elimination reaction  Zaitsev Product => Highly substituted alkene…

Q: Draw the major product of the aldol addition reaction between two of these aldehydes with the…

A:

Q: Rank the following E2 reactions in order of increasing rate. Ph, OTs OTs NaOH NaOH ? NaNH, A Ph.…

A: E2 reaction is bimolecular elimination reaction. Rate = kRXBase, X is the leaving group Rate is…

Q: please place the reagent in the proper order as to complete the below synthesis in a way that…

A: Ans

Q: Current Attempt in Progress The compound below can react rapidly via an Sw1 process: OTS Select the…

A: Solution : The rate of unimolecular nucleophilic substitution reaction (SN1 )depends on the…

Q: show products and mechanism for reaction below: ** O Unel Tommation| (a) Pd(PPH3)4 OMe EtzN (b) 1)…

A: In presence of Pd catalyst,  aryl halide undergo oxidative addition and followed by coupling…

Q: Propose this mechanism

A: Given reaction,

Q: An NH2 group_the ring toward electrophilic aromatic substitution by. a. activates, the inductive…

A: An NH2 group activates the ring toward electrophillic aromatic substitution by resonance. Option "c"…

Q: Addition of excess acid halide to an alkyne would produce a/an ___ dihalide Vicinal       Geminal…

A: Addition of excess acid halide to an alkyne would produce a/an ___ dihalide .. answer is given…

Q: Identify compounds A-G in the following synthesis scheme. Mg(s) A В Et,0 1. 2 2. Н,О, НСІ РСС D Br2…

A: Compounds A-G has to be identified.

Q: Propose a mechanism for cach of the following reactions ОН H2SO4 + H2O ОН

A: This reaction is the dehydration of alcohol by the formation of carbocation as intermediate. Hence…

Q: Which rearrangement product will form preferentially during the [1,2]-rearrangement of an R-group?…

A: The rearrangement product is stable if the intermediate carbocation formed is stable. We have to see…

Q: Q2. For the reactions below, draw out the reactions as shown and answer the following questions for…

A: This reaction example of elimination reaction.

Q: H₂O /H₂SO4 HgSO4 NaBH4/CH3OH

A: Given reaction is :  Predict the products of the reaction ?  According to Markovnikov's rule,…

Q: enolate 人: base enolate base

A: