CI H3C ELOH, NaCN Br H3C DMF ÇI Na H;C CH3 éter

Q: I-O-I I I I-Ò-I I-ö-I 11. Which of the following acts as electrophile in the reaction of benzene…

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Q: a) Complete the mechanism of the initial step of the reaction of the alkyl halide with sodium azide…

A: Reaction mechanism of chlorocyclopentane with sodium azide is drawn as,

Q: What major organic product would you expect to obtain when the molecule A reacts with each of the…

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Q: Predict the product involving the carbylamine reaction? Indicate NR if there is NG REACTION. a. H H…

A: Carbylamine reaction is used to synthesis isocyanide ( RNC) by the reaction between a primary amine,…

Q: 2.4 Me HCI(aq) Me

A: The given reaction is an example of Pinacol-Pinacolone rearrangement of 1,2-diol. The mechanism of…

Q: Pd(OAc)9, 2 PhgP 2 C,H;CH=CH, + I- I (CH3CH2) §N

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Q: Et + CH;0 `Me Alta concentración Br Et + CH3OH `Me Br

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Q: Select the major organic product resulting from the sequence of the reactions written. CH3 Zn(Hg)…

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Q: Which of the following is the product of the acid-catalyzed reaction between acetone (CH3COCH3), and…

A: The mechanism for the acid catalysed nucleophilic attack of methylamine on electrophilic carbon…

Q: (b) Give the product and mechanisms for the following reactions. N. CI CI i) CH3CH₂CH₂COPh,…

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Q: MgBr Mgl (a) + H,C-0 (b) -MgCl (c) CH,-CH + Ph-CHO CH,

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Q: What would be the product of the following reaction sequence? i) SOa, 11) C Hg, AICI3 i11) Zn(Hg),…

A: Note: As per our guidelines, we are supposed to solve only one question. Please repost the other…

Q: Select the molecule which is most reactive towards nucleophilic substitution. NH2 CI но, A в D O A

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Q: Predict the products/intermediates of the following nucleophilic substitution reactions. NaN3 Ph O.…

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Q: Provide a reasonable mechanism for the following reactions: a. m-CPBA b. OH LDA/TMSCI Ph m-CPBA/H30*…

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Q: Draw the major organic product of the reaction shown. CH3OH HẲNCH, CO, HCI • You do not have to…

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Q: Give the major product(s) of the following reaction. PCI3 OH pyridine CI CH, Br to CI Br

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Q: 1. Predict the product and write the systematic reaction mechanism for the reaction of benzoic acid…

A: Carboxylic acids when treated with alcohols in presence of inorganic acid as catalyst results in the…

Q: `N CI NaOH H₂O OH

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Q: Suggest a plausible-mechanism-for the synthesis of the compound shown below H30 OH

A: This synthesis is bassed on Dienone-phenol rearrangement followed by reduction of side ring.

Q: DCC= diaydonexylcarbodimide Ester Yormation RxN DCC HO OH

A: Here is  the mechanism of the ester formation

Q: The following reaction involves cleavage of the sp³C-C=O bond followed by allylic rearrangement.…

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Q: 2. (a) Provide the structure of the product of the following reaction for preparation of an alcohol.…

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Q: Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a…

A: Carbonyl center has electrophilic center hence it can give nucleophilic substitution reaction.

Q: i. H C=0 . Ag(NH,), + -ОН H,0

A: In this question the aldehyde given is benzaldehyde The reagent given is tollens reagent (Ammonical…

Q: Name the products for an SN1 reaction with iodide for the following compound. Indicate major and…

A: for Sn1 reaction-  1st step remove the leaving group, and formation the carbocation 2nd step…

Q: Choose the most appropriate reagent(s) for the conversion of the ketone to the primary amine…

A: H2/ Pd is used to reduce the alkenes present in the reactants. The reaction of NaNH2 and NH3 is a…

Q: Predict the major products formed when 2- methyl-1-butene reacts with: H2, Pt/25°C. Show the…

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Q: Identify the nucleophile and the electrophile in the following acid–base reactions:

A: The polar organic reactions are brought about by two types of reagents. Depending upon their ability…

Q: Write the expected substitution product(s) for each reaction and predict the mechanism by which each…

A: Given:

Q: What is the product of the following reaction after acidic workup? EtMgBr (xs) H3O* OMe А. С. OH В.…

A: When any ester reacts with ethyl magnesium Bromide (or Grignard reagent) then initially an unstable…

Q: ime left 0.00:0 What major organic product would you expect to obtain when acetic anhydride reacts…

A: The esterification reaction is the reaction of an organic acid RCOOH with an alcohol ROH to form an…

Q: COCH3 NaBH4 / H₂O 1. excess LIAIH4 2. H₂O Br Mg/ether 1. 2. H₂O H

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Q: Draw the coupling product of the Pd(0)-catalyzed Suzuki reaction between the compounds shown. Show…

A: coupling reactions :          When two substrates are combined in the presence of a metal catalyst,…

Q: 7. Identify and label the nucleophile and electrophile in the following reaction below. + H-CI CIF A…

A: The species that are either electropositive or have vacant orbitals to attract negative centers or…

Q: Give the major product(s) of the following reaction. OMe H20, H+ heat OMe

A: in reaction 1st the given compopund on tratment with water in acidic medium gives 1 mol…

Q: Draw the product of the reaction shown below. Ignore inorganic byproducts. HO HO Na2Cr207 H2O,…

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Q: Could u show the products and the mechanism of the following reaction and give a short explenation?…

A: No, there is not possible to form product by elemental bromine instead of acidic HBr because…

Q: i) o CH,CH3 • HBr OH Br-CH2CH3 ii) Identify the organic product A, B, C and D in the following…

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Q: Which one of the structures below represents the major product obtained from the reaction shown in…

A: we have to predict the product form for the given reaction

Q: Eto Eto -NH2 5 ELOH 'N. 5a Ph Ph

A: Nucleophilic addition reaction is a addition reaction in which electrophilic triple or double bond…

Q: Name the products for an SN1 reaction with iodide for the following compound Indicate major and…

A: here, Sn1 reaction is given condition of Sn1 reaction- 1. remove the halide ion and formation of…

Q: The following reaction schemes have flaws as presented. Which of the following statement is the best…

A: Given scheme is an example of electrophilic substitution reaction. In this reaction, Friedel craft…

Q: Sn, Conc HCI - OH (j) A B `NO2 (k) NBS, A B "OCH3 hv AICI3

A: The reactions given are,

Q: Na;CO, 0N H2 CH,-C-I 0N. NaI DMF NO NO2 3,5-Dinitrobenzoic Acid lodoethane Ethyl-3,5-dinitrobenzoate

A: The SN2 reaction mechanism involves the nucleophilic substitution reaction of the leaving group…

Q: 4) Predict the mechanism and the reactants to synthesize the following: C. В. A. t 10: :CI:

A: We have find out the starting compound and reagents

Q: Draw the organic products of the following Pd-catalysed reactions, paying particular attention to…

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Q: Give the major product(s) of the following reaction. TSCI CH3CH2OH pyridine

A: This reaction shows tosylation of alcohols and alkyl tosylate has been formed as product.

Q: Draw the major organic product of the reaction shown. (CH3CH2)3N (CH3)2CHCH,CHCOZ…

A: The reactants given in the reaction shown are leucine and di-tert-butyl dicarbonate.  The reagent…

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.