Q: The major product of the following reaction is он H,SO, heat
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Q: For the following structure, (a) propose the starting materials necess it through an aldol reaction.…
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A: Here we are required to predict the mechanism of anisole with bromine with FeBr3.
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Q: Draw a stepwise detailed mechanism that illustrates how four organic products are formed in the…
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Q: ОН HO (a) (b)
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Q: From the given structures which is (a) an acid halide? (b) a secondary amide (c) an aldehyde…
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Q: CI ***** A Et Et Et B Et C Et Et D
A: ->In E2 elimination reaction antiperiplanar beta hydrogen eliminated and alkene formed.
Q: .give the mechanism of given bleow reaction with explanation
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Q: c. Describe (using appropriate figures) one reaction that exploits epoxides as the starting…
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Q: OH
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Q: How to retrosynthesize this compound. Give steps in the foward direction also, with reagents. NH
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Q: Which reagents could be combined to make the following in a reasonable number of steps and order?
A: To determine which reagents could be combined to make below compound
Q: In an unsymmetrical epoxide, the nucleophile attacks at the lesssubstituted carbon atom. Explain…
A: In an unsymmetrical epoxide, the nucleophile attacks at the less substituted carbon atom because of…
Q: 8. Propose an efficient synthesis of for each of the following transformation: a) b) EtO OEt
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Q: Draw the mechanism with curved arrows (Williamson Ether Synthesis). Please provide detailed…
A: Williamson synthesized the ether from alcohol
Q: A. What a combination of Grignard and carbonyl compound can be used to prepare the following…
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Q: how does the TMS group leave? and leave only a Oxygen. please draw as a mechanism.
A: The mechanism of leaving the TMS group in the given reaction happens as follows.
Q: what is the mechanism of p-nitroaniline ??
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Q: Please Complete the following reaction with Major Compund with explaination in handwritten....
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Q: a) b)
A: Applying reagent and suitable chemical reaction As LDA RMgX etc.
Q: What product is formed when A is treated with Grubbs catalyst underhigh-dilution conditions? This…
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Q: Give a clear explanation handwritten answer...give the mechanism for Friedel acylation with curved…
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Q: Grignard reactions are often limited by steric hindrance. While Grignard reagents react in high…
A: Grignard reagents when react with epoxide then major product formed is a primary alcohol.
Q: Propose mechanism consistent with the following reactions a and b.
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Q: Arrange the following compounds according to their rate of solvolysis with suitable explanation.
A: SN1 reaction: SN1 stands for nucleophilic substitution first order, where the rate of reaction is…
Q: A. What a combination of Grignard and carbonyl compound can be used to prepare the following…
A: The synthesis method for the two given compounds has to be given.
Q: Please provide complete explanation. Thank you! Is recrystallization necessary in synthesizing…
A: Interpretation- We have to tell that , Is recrystallization is necessary in synthesizing…
Q: 7. Propose an efficient synthesis of for each of the following transformation: a) b)
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Q: base ? A B
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Q: The molecule below reacts with the primary amine Ena-NH, and undergoes a retro-aldol type reaction…
A: Given reaction:
Q: HBr peroxides
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Q: Propose a mechanism for the following reaction. КОН in MeOН
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Q: Could you explain the main characteristics and occurences in nucleophilic acyl substitution? Thank…
A: Nucleophilic acyl substitution describe a class of substitution reaction involving nucleophiles and…
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A: The ether is formed by Williamson's synthesis which is proceeded by the reaction of an alcohol with…
Q: You have learned two ways to make an alkyl benzene: Friedel–Crafts alkylation, and Friedel–Crafts…
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A: The detailed mechanism with explaination for the above two reaction is provided in a attached image.
Q: (b) Provide forward reaction) compounds provided : (i) (ii) NC suitable retrosynthesis for the CN as…
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Q: 17. Provide a curved arrow mechanism for the following transformation. Br NaN, DMSO
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Explain in details the mechanism of preparing B-ionone from first step till last step. Please write in details ??
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- Why do you suppose ketone halogenations in acidic media are referred to as being acid-catalyzed, whereas halogenations in basic media are base-promoted? In other words, why is a full equivalent of base required for halogenation?Which g the foellowing Strategis ayld yıcld an est« ?. 9 Nuckophilic qcyl Substitutiun q an acid Chluride with an alcoho) b) Reactwn y a O Nucleophilic acyl substitu tion of an J All of the abuve Carbuxylıc aud and an alcohel with Catayhe Sulfuriè acıd anhydale. with methand) Which nitrogen atfom B the p strongest by se ( Cirak A, B, or c)? Aphenylfulvene Mo t Moleic to that 6. produce bub white broduct 10/our c0/0rless the of it has white nana e po duct gtoe explain 2710 but red. not ahe of this reactHon. assa
- Write the missing product or reagent in each of the following: En0; Eno CO₂Me OH I ?????? OTT 1) p Ts OH (cat.), Me OH CH₂Cl₂,rt. 2 h (98%yield) 2) 1) NaBH4 2) NH₂Cl(aq) 3) NaI0, Bu NBT (COCI), DMSO E₂N, -78°C ACO OAC I-OAC 0 LCHO19. Mechanism cat. TSOH H. CH;OHProvide a stepwise synthesis of 1-cyclopentylethanamine using the Gabriel synthesis. NH NK NH HO. OH NH2 Кон; ;H3O+ KOH; ;H30* "Br LIAIH4; ; H3O* Br LIAIH4;
- ent Predict the major product when the compound labelled W below is treated with mercuric acetate (Hg(OAc)2) and H₂O, followed by sodium borohydride in base (NaBH4, OH). OIV Oll OV -Ph OH + enantiomer 11 Ph HO. -Ph W OH + enantiomer ||| НО. -Ph IV -Ph HO V -Ph NextProblem 16 of 85 Submit Draw the major product of this reaction. Ignore inorganic byproducts. ¿ Q 1. LDA, -78 °C 2. CH3CH2Br (1 equiv) Select to Draw >What is the final organic product in the following sequence of reactions? & Oll O III ON OV но. 1 H* OH & & & & 1. DIBAL-H 2. H₂O* III IV CHÍNH mild acid HN
- We your anver on paper and submit a picture here gir emaitto me ty the end of pe time for he exam CHOH CH.OH CHOH HA Provide a step-wise mechanism for the following equation, show intermediates and arrows for exchange of electrons.Which of the following reagents should be reacted with the reactant to get the given product? Select one: a. ethanamine; LIAIH, diethyl ether, H₂O Ob. NaOCH₂CH3; H₂in Pt OC. methanamine; NaBH, O d. methanol; DIBAL, H₂0* Br H to trLout line a synthesis tor geherating Compand ma as the excusive using Compounds Fan 6. LDA or as your Selečtish ofbases major priduct You may ust only Number es sential Steps as requiree trans farmation the Componnd