Predict the major products of the following. (c) (a) (b) HO,S ? HNO3 Cl2 ? FeCla AICI, H2SO, H,CO (e) (d) Conc. HNO3 Br2, ? ? FeBr3

Q: chem 534 cha Hư OAc please show stereochemistry H₂COCH ? H + H H- CO₂CH3 2. 0Ac ? hv= ? 40°C 3. H₂C…

A: “Since you have posted a question with multiple sub parts, we will provide the solution only to the…

Q: Consider the following pericyclic reaction. CH3 H3C H. `H H3CO/ H3C H3CO `CH3 K L (a) Name the type…

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Q: Br -OC(CH3)3 а. b. -OCH,CH3 CI CI с. "NH2 (2 equiv)

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Q: Predict the outcome of the following reactions and explain the reason briefly.

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A: Mechanism is given below in next step

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A: Oxymercuration-demercuration is a organic reaction that can be used to convert an alkene into an…

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A: The reaction mechanism adopted in the given reaction has been described below.

Q: HN03 NO lely (A) ( B) NAI,-NH, BY OF

A: The organic syntheses are carried out with the help of reagents. These reactions are carried out in…

Q: Hg(OAc), PDC (xi) HCI, H,0 OEt CF, CH, HNO, H,So,

A: Ans

Q: Give the major organic product(s) of the following reactions (a-e).

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Q: 2) Complete the following: Stereochemistry and reg a) MeO₂C b) c) d) *** type type type type NH₂…

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Q: Provide the reagents in correct order necessary to carry out the following conversion. OCHS Br NO,…

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Q: Rank the following according to DECREASING reactivity towards E2 Br H,C. CH, Br H. CH Br H,C. CH Br…

A: In E2 elimination, a double bond is formed by elimination of the leaving group and an H in the…

Q: None

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Q: Draw the structure of each molecule. (a) (E)-4-carbamoylbut-3-enoic acid; (b)…

A: Since we answer only upto 3 sub-parts, we'll answer the first 3. Please resubmit the question and…

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Q: 2 Use FMO and aromatic transition State theories [y + + 2a] and [4 = ²2²] TT S Egcloaddition…

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A: These are the examples of electrophilic addition reactions

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Q: Arrange the following compounds in the increasing order of reactivity in SN' reaction. 1.…

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Q: What is the likely product of the SN2 reaction shown? OH

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Q: 134. The major product formed in the following reaction sequence is: OMe (1) (CF;CO),O; NE13 (A) (2)…

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Q: Draw the starting material that, under the given reaction conditions, results in the following…

A: The objective of this question is to draw the starting compounds in the given reactions.

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Q: 1. For the following reactions, predict the major product. lio peroxides). peroxides H2504 C) A H20

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Q: (CH),CuLi CH3 b) HOCH,CH,OH CH3 c) H,NNHC,H, HC. CH3

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Q: what is the SNa,SN2 , and Ez Of this Pigme? which is most Linely to occur? Please incluele their…

A: SN1 Reaction: The SN1 reaction is a substitution nucleophilic unimolecular reaction. It is a…

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A: The mechanism for the following reaction is -

Q: The stereochemistry of the following alkenes are? QH CH2 or b. с. (A) a: Z; b: Z; c: E; d: E (D) a:…

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Q: for the Cl2 addition reaction with 1,2dimethylcyclohexene, draw the most reasonable curved arrow…

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Q: (а) FeCl, (1) NANO, HCI (b) 0-5 °C NH2 () CuBr (1) BH,. THF (с) (i) NaOH, H,O2 KMNO, (d) heat

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Q: Arrange the following compounds in increasing reactivity towards Et. CI Select one: a. O b. O C. O…

A: -> Benzene substituted compound give electrophilic aromatic substitution reaction. In this…

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Q: Explain why each of the following reactions will not proceed as written. a. + CO2 COOH b.…

A: Substitution reactions occur when an atom or a group of atoms is replaced by another atom or group.…

Q: Which carbocation would be the most stable? OI O II 00 ||| ONV OV + H II X d + III + IV V +

A: It is the overlapping between C-H and * or  *C-H and  orbital.

Q: Prediga los productos de las siguientes reacciones. (a) éter sec-butil isopropflico + HBr conc.,…

A: Given in following question mantion reaction predict product give below reactions  and explanation…

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.