The Swern Oxidataion, PCC or NaOCl with TEMPO will convert ___________ to a terminal carbonyl.     hexan-3-ol     pentan-2-ol     heptan-3-one     butan-1-ol

Q: 6. What is the best choice of reagent(s) to carry out the ? transformation shown here? Ph HO. Ph A)…

A: We have given three organic reaction we have to find major product obtained from these reactions.

Q: OEt Drag the appropriate labels to their respective targets. Rese H H H. NaOEt NAOH Ph Ph OEt EtO…

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Q: Draw the products of the given reaction. Include all appropriate hydrogen atoms and charges. Draw…

A: In this reaction mechanism, amine Compound abstract H+ ion from the water and give Ammonium salt as…

Q: Draw the product formed when each organometallic reagent is treated with H2O.

A:

Q: H20 `CI

A: It is a tertiary alkyl halide. Hence, both SN^1 and E1 reaction will be favoured. But, water is a…

Q: Draw the product formed when the α,β-unsaturated ketone A is treated with each reagent.a. NaBH4,…

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

Q: Draw the structure corresponding to each name.a. 5-methylheptanoyl chlorideb. isopropyl propanoatec.…

A: Hi there! Since there are multiple subparts in the question, we will answer the first three for you.…

Q: Draw the products of each reaction. NANH2 NaOH KNH2 b. CH,0- -CI a. NH3 H20 NH3 A

A: Elimination-addition reaction: To carry out substation in haloarenes drastic conditions such as…

Q: MULTIPLE CHOICE QUESTION Which Wittig reagent is necessary to complete the following transformation?…

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Q: Draw the product formed in each reaction. [1] NANO2, HCI [2) CuBr [1] NaNO2, HCI [2] HBF, -NH2 c.…

A: Since you are posted with multiple sub-parts. As per the rule, I am answering the first three…

Q: CH3NH2 H30* e) j) NaOEt Aldol Condensation

A: Given reactions,

Q: Draw a stepwise mechanism for each reaction. Br + CH3CH2NH2 NaOH 'N" + H20 + NaBr a. Br ČH,CH3 NABH4…

A: When aldehyde or ketone reacts with NaBH4, they get reduced to alcohol. Cyclization is defined as…

Q: HCI 0°C Draw the major product.

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Q: 2 CH3COOCH,CH3 C2H5O°K"/C2HSOH ---> CH3COCH2COOCH2CH3 +] Hofmann elimination Clemmensen reduction…

A: The above given reaction is a claisen  condensation. Claisen condensation is a organic coupling…

Q: Draw the product formed when each organometallic reagent is treated with H2O.

A: (a) Cyclohexane is formed by the abstraction of a proton by cyclohexyllithium from water molecule.…

Q: 1.What is the best reagent to complete this synthesis? OA 1)???? CN 7.) NaCN.

A: Since you have posted a multiple questions in a single session, we are entitled to answer first…

Q: H2 H,0, H* CH3 H3C. H2C 1. CH,

A: This compound is a ketal having two different alcoholic arms. So, after hydrolysis it produces two…

Q: Draw the products of the complete hydrolysis of an acetal. Draw all products of the reaction. 애 H…

A: Carbonyl compound (aldehyde and ketone) reacts with alcohol to form hemiacetal in the presence of an…

Q: Which is a synthesis of 3-bromohexane? 1 eq. Br2 H2. Lindlar NaNH2 1 ед. HBr H2, Pd/C NaNH2 1 eq.…

A: Here in the given reaction, 1-butyne is converted to 3-bromohexane through a number of steps.…

Q: Acetal product formation is difficult, since hemiacetals are stable while acetals are not stable.…

A: In this question, we will see this given statement in the Question is true or false.  We will…

Q: Provide the synthetic route for the following reaction?  (CH3)2CHCH2Br ----> (CH3)2CHCH2CH2CH2NH2

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Q: Draw the complete arrow pushing mechanism for the base-catalyzed keto/en the following compound.…

A: The chemical equilibrium between ketonic and aldehydic form of same substance which get formed due…

Q: Draw the products formed when A or B is treated with each reagent. In some cases, no reaction…

A: Hello. Since the question consists of multiple sub-parts, the first sub-part shall be only solved.…

Q: Draw the products of each reaction. CHO Br. OCH3 Br2 so3 a. -CN i. H2SO, FeBr3 H2SO4 CH3 NaSCH,CH3…

A: Note: Since you have posted a question with multiple subparts, we will solve the first three…

Q: Draw the rearrangement-elimination product of 2-ethyl-3-methyl-2-(1-methylethyl)butan-1-ol, sulfuric…

A: In presence of strong acid and heat, water molecule leaves out the system and carbocation is formed.…

Q: Complete each multi the way. Synthesis A 1) Br2, H20 2) Nao only one stereoisomer required 1) BrMg-…

A: Soln

Q: Br KCN Select one: Primary alkyl halide; SN1 reaction mechanism. Primary alkyl halide; SN2 reaction…

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Q: 1NODET roomteme 2. CH3 CH2B (1 equi)" Enolate Anion + Katone Aldehyde OH 1. NAOH 2.neut wakup…

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Q: Draw the products of each reaction.

A: a) Please find below the reaction taking place.

Q: Draw the neutral product. Select Draw Rings More Erase H CI excess NANH2

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Q: 2 NaOH Hz propan-2-ol CH;NH, но CH3 PCI5 propan-2-ol NaOH(aq) Tollen's reagent LIAIH,

A: Organic reaction mechanisms:

Q: Draw the keto- tautomer for the following enols

A: Tautomers have two form keto form and enol form both keto and enol form are in equilibrium with each…

Q: Which reaction will not give 100% enolate? to EtO OEt LDA NaOEt H. NaOEt EtO LDA

A: In this question, we will Identify the Reaction which doesn't give 100% enolate. How we can solved…

Q: SN1 SN2 Br YES (example) (ехample) SECONDARY (SUBSTRATE) YES YES TOSYLATE (OTs) GOOD (LEAVING GROUP)…

A: ITs entirely  depends  upon the  Reaction  conditions whether an Sn1 or Sn2 Reaction  will occ.

Q: Draw the major product of the following reaction sequence. OH H2CrO4 HO NaBH4 H*/H20 ELOH он H3C* но

A: Explanation step wise .

Q: Choose the correct product of the following reaction. A Ph- -CH2CH3 H H Select one: Ph CH2CH3 Ph…

A: Given,

Q: O Provide the correct stuchre for intermediates A-M ) Mez Culi Socz NACN Br B PYndime D 2) H20 DLAH…

A: In organic chemistry, inter conversion of organic molecule takes place from one form to another form…

Q: - Which Wittig reagent is needed to accomplish Ths formation? Witt. reagent d Ph, As clstaXosa} a)…

A:

Q: Given the follówing proposed mechar reaction. 2A+ 2B C+2D step 1: 2A+B-C+E(slow) step 2: E+B-2D…

A: In any given reaction, slowest step is the rate determining step that means rate of reaction depends…

Q: NABH4 CH3OH + H,O NH2 Draw the product of each step. NH2 draw structure .. proton transfer

A: Applying concept of reduction followed by proton transfer and cyclisation reaction.

Q: What is the main product of the following reaction sequence? CH3CH2Br HCI ? H2O trace H* H3CH2C.…

A: Here, the first step is the formation of enamine. Cyclopentanone reacts with pyrrolidine in presence…

Q: Aldol Mechanisms: Synthesis of 2-ethyl-hex-2-enal

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Q: Which compound is the major product of the reaction sequence shown? (1) SOC2 (A) (B) HO. (2)…

A: Given is two step reaction.

Q: Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: HBr OH Br Part 1:…

A: In the given reaction alcohol is reacting with HBr to give alkyl halide as the product, In the given…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. CH3CO2NA Select to Draw

A: Esterification reaction: An acid chloride reacts with sodium carboxylate to form an ester, the…

Q: Draw a stepwise mechanism for the following reaction: HBr HO, Br Part 1: HOBR Br H20 HO view…

A: Given reaction is preparation of alkyl bromide from alcohol  It is an example of nucleophilic…

Q: Consider the synthetic sequence shown. Identify the reagents Br for all three steps. Draw the…

A: We have to first convert the benzyl bromide to Benzyl magnesium bromide and have convert it to…

Q: Br NaOH heat Draw E1 Major Product + Draw Minor E1 Product

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Q: Draw the product formed when each organometallic reagent is treated with H2O.

A: Organometallic chemistry explains the chemistry of compounds containing metal-carbon bonds. An…

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.