Show Steps for Mechanism and Box Final Product D HBr, ROOR La) 2 PP hg 3) Buli 4) (CHg)z C =0 ) Mg, a ether 2) CH3 CN Br 3) H30* 1) CH3 MBr, ether 2) HzO* 3) H2 304

Q: Supply the missing compounds in the following synthesis scheme. 1. NaNH2 (3 equiv) H CCI4 Br2 1.…

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Q: Mechanism 1. Propose a mechanism that accounts for the transformation below. TSOH, EIOH EtO…

A: This reaction proceeds through SN2 mechanism.

Q: )CHz MgBY 2) AQ. Workup 3) PBY3 -CH3 Br

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Q: Consider the interesting cascade transformation below. Provide a detailed mechanism including all…

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Q: Provide mechanism and major organic product. 1) NaOCH,CH3' CH;CH2OH 2) H30*

A: Given reaction is interanolecular reaction

Q: The carbon adjacent to a nitrile group (CN) can be deprotonated using LDA and alkylated with an…

A: Applying concept of organic synthesis.

Q: i-step synthetic pathway below by filling in the missing products along Synthesis B Synthesis C…

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Q: Show the Reaction of a 1° ROH with HX—An SN2 Mechanism ?

A: SN2 Mechanism refers to a bimolecular nucleophilic substitution mechanism. Ex: ROH + HX -> RX +…

Q: Consider the reaction scheme shown below. HCI [1] HO. (a) Provide a detailed mechanism for reaction…

A: This reaction will occur via 3 step. In first step protonation then Water molecule eliminate to…

Q: Predict the product. No need for full mechanism. answer all for upvote Br KNO3, H2SO4 Br NANH2 В.…

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Q: 'Br Br NaCN 1. LIAIH4 2. H₂O NH₂

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Q: + Naz BOz NABHY (CH3)2CHOH

A: NaBH4 is a reducing agent that can reduce aldehydes and ketones.

Q: What are the major products of these reactions (pls show the mechanism so i can understand how to do…

A: Hello. Since the question contains multiple subparts the first three subparts are solved. In case…

Q: Br NaOCH3

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Q: H+ CH;OH heat OH

A: Organic reaction mechanism.

Q: Br HBr

A: available lone pair on O-atom acts as lewis base, H+ acts as lewis acid and lewis acid-base reaction…

Q: OH p-TSOH, C6H8

A: In this reaction, firstly carbocation is generated then ring expansion take place then base abstract…

Q: Br. SO3H

A: Ans  Electrophilic substitution reaction initially sulphonation then bromination of benzene

Q: Br KNO3, H2SO4 A. А. Br NaNH2 `N' В. SnCl4 CI С. ZI

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Q: Consider the interesting cascade transformation below. Provide a detailed mechanism including all…

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Q: 6. Br2, aq. NaOH `NH2 1) LDA 7.

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Q: Br NaOEt ELOH

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Q: Propose a reasonable mechanism. H*/ H2O

A: Given reaction,

Q: a) Carry out the following transformation and provide mechanism. C,H; CH: H a) H.C. C NH2 -COOH Ph…

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Q: Bonus: Propose a mechanism Must be perfect for any points NaOEt OEt EtO EtO HOE!

A: Given reaction,

Q: CH3 1) Hg(OAc)2 H;0 а) 2) NABH, H3C CH3 1) BH, 2) H;O-H¿O

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Q: OH 7.

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Q: Propose a mechanism for attached reaction:

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Q: Which mechanism is consistent with the reaction below? (CH3)3CBr+OH-→(CH3)3COH+Br-   1.…

A: Carbocation can be defined as the species in which carbon atom bear positive charge. It can be…

Q: CrO3, H2SO4 acetone

A: CrO3.H2SO4 also known as Jones reagent which is used for oxidation .It oxidizes primary alcohols to…

Q: 2) Propose a mechanism for the following reaction (show all arrow pushing). Note that DgO* has…

A: Two molecules which have same molecular formula but different connectivity and they are easily…

Q: Show the mechanism for the reaction conducted at-5 "C in CCI,. cyclohexene + bromine…

A: Given reaction is addition reaction.

Q: 1. EtMgBr A 2. H*, H20 1. (Et)2CuLi 2. H*, H20

A: The mechanism of the following is:

Q: Mechanisin: Which mechanism below is depicted correctly? Pho Ph Ph :0: Ph Ph + (Ph)3P=0 + Ph HH HH…

A: The mechanisms given are,

Q: HN CH3B H,0 H* (cat)

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Q: НО NaOH (CH3),N (CH3),NCH,CH,CI Can you show this mechanism please?

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

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: Draw a detailed, step-wise mechanism for the reaction shown below. SHOW ALL BOND-FORMING AND…

A: In the above reaction, the OH- present in the base NaOH will attack on the carbon making ester bond…

Q: NH2 ii) Me

A: Here we have to synthesize the following given compound from starting material aniline through…

Q: Carry out following conversion. Provide suitable reagents, reaction conditions and also mechanism…

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Q: CH3 HO OCH3 CH3 HO, ČH3 OCH3 H* Ph ACTUAL PRODUCT

A: H+ is catalyst here,it promotes the reaction by increasing the electrophilicity

Q: 3. Provide full mechanism (curved arrows and intermediates) for the following reaction. OCH3 1.…

A: Answer 3 )  The mechanism for the given reaction = ?  Note : As per our company guidelines, we are…

Q: H3CO, NaOH H,CO H3CO OCH3

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Q: N. Br2/FeBr3 CO2CH3 SO/H2SO4 HO. CI AICI3 NO2 HNO3/H2SO4 CN

A: Reaction 1 : EAS (Bromine electrophile). Reaction 2 : Sulphonation ( SO3 electrophile). Reaction 3 :…

Q: Provide mechanism and major organic product. 1) NaOCH,CH, CH;CH,OH 2) H,0 d.

A: This question is related to finding out the major product in the organic reaction. Follow…

Q: (d) Br. HCI (е) H3CO HCI H3CO (f) F3C HCI F3C

A: We need to form the product from the given  alkenes that react with HCl. The products and reaction…

Q: NH2 Ν H2NΝΗ2 CH3 H+

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Q: nothe Write a detailed mechanism for this transformation но. HCI HO H20 H

A: The given reaction is an hydrolysis of ether

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.