When a Grignard reagent reacts with a ketone, the product of the nucleophilic addition reaction is what type of alcohol. Choose the type of alcohol product? А. CH,-ҫн— сн-он ČH, OH В. CH,-CH-CH, OH он С. CH,- CH-CH;-CH, OH CH,- CH;-C-CH, CH,

Q: CH;CH,CH=PPh; -Propanol 2-methylpentan-3-one H+, heat H2N°

A: Applying concept of organic synthesis of compounds.

Q: Draw a structural formula for the alkene with the molecular formula C5H10 that reacts with Br2 to…

A: The Bromination of alkene occurs through an intermediate bromonium ion. The compound 1,…

Q: 1. The first step involves 2. H-CI is polarised: H is the 3. The alkene behaves as a 4. In step 1,…

A: The reaction of an alkene with hydrogen halide proceeds through two steps.The first step is the…

Q: Give an acceptable name for each aldehyde.

A: According to IUPAC rules the name of compounds a) 3-methyl Hexan-1-al b) 3,5-dimethyl heptan-1-al c)…

Q: h) OH CH3-CH-CHCH₂CH3 CH3 H3O+ fl CHO-CHIC-CHacHtH-O-H CH3 major product CH=CH-CH-CH2CH3+H-O-H 1.…

A: Alcohols on treatment with acid produces carbocation with the loss of water molecule.

Q: What carboxylic acid would you reduce to produce the following alcohol? H3C H3C CH3 OH . You do not…

A:

Q: Give the major organic product of the following reaction. 요 CH3CH₂ CH3CH₂ CH₂ CH₂ CH3CH₂ CH3 O= OH…

A: When Carboxylic acid reacts with SOCl2 then it forms acid chloride which on reaction with alcohol…

Q: Which one is an acetal?

A: Acetals are geminal-diether derivatives of aldehydes or ketones, formed by reaction with two…

Q: What is the product of this reaction? 1. LiAlH4 ??? не от 2.H+ ОН ada d Н н (В) (D) (A) ОН ОН ОН

A:

Q: What are the products of the following reaction? H, heat, CH,-С-он CH-он

A: When alcohol reacts with carboxylic acid we get the resulting product to be an ester.

Q: Which alcohol is formed from the acid-catalyzed hydration of the following alkene? H CH3 H,0 H2SO4…

A:

Q: 35. The products of the following reaction are معلمه CH,—CH,COCH + NaOH NO-OLON. ??-?? 0-01-01 C)…

A: This is an example of basic hydrolysis of ester.  Carboxylic acid cannot exist as COOH in the…

Q: Consider the formation of n-butyl bromide from the reaction of n-butyl alcohol with NaBr and H₂SO4.…

A: The reaction of n-butyl alcohol with NaBr and H2SO4 form n-butyl bromide is shown in the given…

Q: | 2. Name and draw the product produced by the oxidation of each compound. (а) CH,— СH,— CH,—…

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Q: Which of the compounds is/are hemiacetal, acetal, hemiketal and ketal?

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Q: Determine the products of each carboxylic acid reaction. a. CH3-CH2-CH;-CH-C-OH + CH, — CH,— он…

A: In this, the product of the given reaction needs to be drawn, 1) First is an esterification reaction…

Q: Which is the starting material in the following reaction? ? A) C) 1. (CH3)2CuLi 2. H₂O i B) D)

A:

Q: Which one of the following compounds would react with CH3CH2MgBr, followed by acidic hydrolysis, to…

A: This is multiple questions so I will solved first question for you.  You can see the details…

Q: What reagent is necessary to complete the reaction? H-OH CH₂ CH₂ CH-C CH3 O NaO O NaCl O Na O NaOH +…

A:

Q: What type of reaction is occurring Ester O H CH₂-C N- H+ HOH + HCI O CH₂-C 0 H 11 CH–CH,-C-NCH, +…

A: #1: What type of reaction is occurring: #(a): The reactant is an amide (R-CONH2).

Q: Choose the most appropriate reagent(s) for the synthesis of 1-butyne from ethyne. reagent(s) H = -H-…

A: let see the mechanism step by step

Q: Reactions: 20) cis-4-bromo, 3-methyl, 2-pentene undergoes chlorination. Name final product. 21)…

A: Here we are required to find the product of the reaction .

Q: aldehyde CH,- CH = 0 CH2 О3D С — С — Н CH3 NH,–C=0 - CH3 CH, CH; – CH, — CH,— С — Он - -

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Q: Which is the major product of this reaction? || CH₂ONa CH2=CH-C-C6H5 CH₂OH

A: Approach to solving the question: Detailed explanation: Examples: Key references:

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.