The following reaction yields TWO main products. Select the correct answer respecting these products (see below). KI TWO major products obtained H;PO, A and B. and and and D. A is correct Dis correct Bis correct Cis correct

Q: • P and R are optically active compounds. Draw the structure of PQ)and R.) (B)H P/CH16 shag Q. C,H18…

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Q: NaOMe МеОН A B D E F What are the two starting materials? of

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Q: How do I synthesize a mechanism

A: The retrosynthetic synthesis involves bromination of the compound followed by elimination reaction.…

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Q: ) Which major product for rxm below? HCN ? KCN NH OH a) )人

A: HCN is a nucleophile. During nucleophilic addition, it breaks into H+ and CN- ions.

Q: Ql- Arrange the following carbonium ion as more stable. Why? Me Me Me A B

A: Since you have posted multiple questions, we are entitled to answer the first only.

Q: The major product formed in the reaction below is:

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A: The given oxidation-reduction reaction is to be balanced-Sn2+ (aq) + IO3- (aq) →Sn4++I-

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

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Q: For each of the tolowing reactions predict the major product. NaOH H,0, A Raney N. A préssure OH…

A: “Since you have asked multiple question, we will solve the first question for you. If you want any…

Q: он HO ČHO ABC DEF GHI

A: ->Reaction of ether with HI produce alkyliodide and alcohol. ->For strength of acids we see…

Q: Provide the starting material. LiCu ОН OCH3 CI A B D E = A or B F = B or C G = none of these

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Q: 6) Which structure best fits the IR shown below? HO. H. a. b.

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Q: 1. Arseric can be extraced from ts ores by fist racing he rewith oxygen (called rasting o form soid…

A: (1) Given that -  Following Equilibrium Reaction -  As4O6(s) + 6C(s) <==> As4(g) + 6CO(g)…

Q: CI cl cl A. (27,47)-2,3,4 trichloro hept-2-ene B. (22, 4E) -2,3,4-tri chloro hexa -2,4-diene 0₁ (2E,…

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Q: Which choice below best describes the following process? 5-² 15-1 Al Qxidation with loss of he B)…

A: Given: S-2→S-1 To find: if oxidation or reduction is taking place.

Q: O b only

A: Answer-  b only

Q: A. Predict the product with configuration OAC AcO AGNO HBr Aco E. A Меон B Aco ACOH

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Q: What is major product choose from A, B, C, D , E

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A: Chromic acid is a fairly straight forwed reagent. It oxidizes primary alcohol to carboxylic acids…

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Q: Predict the product for the following reaction. CN will ON + NaCN

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Q: .CI + AICI; A. D

A: Friedel-crafts alkylation reaction: It is an electrophilic substitution reaction between Arene…

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A: In presence of Na and NH3 , it undergos Birch reduction.

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Q: I GIVE COMPLĒTE MECiHANvism of FelliviNG REACTIONS (Answer any 4) A HBr -BY

A: Hi! Thank you for the question, As per the honor code, we are allowed to answer one question at a…

Q: choose the comect opfion Identify the mast likely product s em conting P to aeas was 8. A) B)

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Q: Fe"(aa) FESCN?" (Blood red) + SCN (aa) (aa) Reagent Effect on species in the equilibrium Fe"(a) SCN…

A: Given: Table  To find: To complete the given table on the basis of Reaction direction Solution:…

Q: Drawthe MAJOR product(s) of the followingreaction. 1) O3 2) DMS 3) excess LAH 4) H2O 1. 1) Hg(OAc)2.…

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Q: hich of the following S Br N

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Q: Draw the Products and D. DI BAI- excess

A: As you have posted multiple questions in a single request, we will solve the first part for you. To…

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Q: Shaw haw T compaunds YOIC a.Smm cauld prepare the fallauing materials with the starting shawn and…

A: Hi, since there are multiple questions posted, we will answer first question. If you want any…

Q: Cl, -CI HCI light b) Which reaction represents the more efficient way to synthesize…

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A: SN1 reaction take place through carbocation intermediate.The 3 degree carbocation is most stable…

Q: AICI . (A), Product (A) is :- whynet Ph HO (B) HO (C) (D)

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Q: the starting material for these two reactior? The rogenation is done first, foßowed by the…

A: The reaction conditions are hydrogenation followed by bromination to give the saturated trans -…

Q: Drawthe MAJOR product(s) of the followingreaction. 1) ВН-THF 2) H-О2, NaOH 3) РСС, СH-Cl 1. он 1)…

A: Given that : We have to draw the major products of the following reactions :

Q: Rearrange the equation to isolate a. (a + ) (d – e) = f a =

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Q: llowing reaction and show all relevant termediates. H2 SO4 Methanol HO

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Q: 2. Which compound(s) in #1 is/are oxidizable(s)? Draw the oxidation products using K2Cr2O7. Ans to…

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Q: What is each compound’s systematic name?

A: Since you posted question with multiple sub-parts, we are entitled to answer the first 3 only.…

Q: 22. Please show step by step solution.

A: The given reaction is addition reaction. Please find the mechanism below.

Q: two products Select Draw Rings More H Br CI Br2,

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Q: 17) (1) Obtain major product(s) for all electrophilic are HNO (A) H₂SO4 (B) (C) O₂N CO₂Me SO 3 H₂SC…

A: In the given question we have to do the following reaction.

Q: Rank the following from worst to best leaving group: * H3Cco® H;CO B HOO I II III IV

A: The order would be:

Q: (vi) Explain the differing reactivity in the two reactions below: H2/Pt Cd CO CH2 1 At., RT. Cal CO…

A: first reaction - H2/Pt means hydrogen electrode which has Platinum. Platinum metal is a catalyst…

Q: Please show how to solve

A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…

Q: H. FS SH

A: Given reaction is acid- base reaction.

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.