Give all possible hydration products of 3-methyl-1-hexyne. Show reaction and reagents

Q: HO (c) Alkene + Reagent HO (d) Alkene + Reagent

A:

Q: Propose two different methods to synthesize 1-octen-3-ol [CH3(CH2),CH(OH)CH=CH] using a Grignard…

A: Solution- The reaction of a Grignard reagent with a carbonyl compound produces alcohols. The general…

Q: Arrange the organic compounds according to increasing polarity. Give a brief explanation for your…

A: Polarity in organic compounds: The polar molecules are the one in which the molecule/ chain consists…

Q: ii) 2-methyl-pent-1-ene 2-methyl-pentan-2-ol

A:

Q: NH2 h. CH (excess) NH i. 1) KOH 2) NH 3)H,N-NH,

A: I am drawing only major products (as written in the question).

Q: Give the IUPAC name of the alkyne that produces only propanoic acid (CH3CH2CO2H) when treated with…

A:

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

A: 20) IUPAC name of product formed is :- 2-bromo-3,4-dichloro-3-methylpentane

Q: 11) Synthesize 2-methyl-3-hydroxycyclohexone from cyclohexone, methyl iodide, and inorganic…

A: We have to carry out the synthesis of 2-methyl-3-hydroxycyclohexanone from cyclohexanone, methyl…

Q: Explain briefly how the following synthesis can be carried out in the laboratory.

A:

Q: 1. Write in the correct reagents to accomplish these reactions. a) 2-methyl-2-pentanol b)…

A:

Q: Mercury-catalyzed hydration of internal alkynes produces a ketone. True/False

A: When internal alkyne is treated with mercury in presence of acid so found the ketone that's why the…

Q: Draw the structure of the given compound. Identify if the given name is correct of incorrect. If…

A: In this question, we have to draw the structure of the given compounds and also name the correct…

Q: 3. The following compound is used in perfume because it smells like lily-of-the-valley. a) b) OH…

A: The IUPAC name of the compound can be written on the basis of the number of carbon atoms in the main…

Q: 111

A:

Q: how to synthesize cis-1,2-cyclohexanediol

A: The question is based on the concept of organic reactions.   We have to convert the reactant into…

Q: 12) Synthesize 2-methyl-prop-2-enal from organic precursors with 2 or fewer carbons and inorganic…

A:

Q: QUESTION 15 Use these findings to answer the question. Compound X is optically inactive and has the…

A: Reductive ozonolysis gives aldehyde and ketone as a product... But in case of oxidative ozonolysis…

Q: DISUBSTITUTED BENZENES Draw the products of monosubstituted benzenes 2-5 with reagents (a)-(f). Cl₂,…

A: Preparation of Disubstituted benzenes:The incoming substituents oriented by the substituents which…

Q: what product is formed in this reaction? 10-07FM What product is formod (Ch₂ Ch 3) 3 N (1/11 (1

A: Although tertiary amines are tending  to be less nucleophilic than secondary amines, they are still…

Q: Identify the functional group and the IUPAC name for each of the three compounds in the reaction…

A: Answer:When primary alcohol is treated with a carboxylic acid in the presence of sulphuric acid, an…

Q: Show how to convert ketones and aldehydes to other functional groups, anddevise multistep syntheses…

A: SOLUTION: Step 1: The aldehydes and ketones can be converted into other functional groups like…

Q: CH;CHOHCH CH: (2) CH:COCH:CH: ZnHg), conc. HCI (3) CH:COOH (4) CH:COCI (5) N-methyl acatamide

A: 1. In presence of oxidising agent (H2Cr2O7),  secondary alcohol converts into ketone.  2. In…

Q: OH CH3 OH CH3 CH3 CH3 OH CH3 OCH3

A: Organic reaction mechanisms.

Q: 1. List the following alcohols in order of increasing reactivity (least reactive first) toward…

A: As per our guidelines, I can only answer first question because you have posted multiple questions.…

Q: The IUPAC name for the hydrocarbon: CH3-CH₂-CH₂-CH-CH₂ - CH3 O 3-benzylhexane O 3-phenylhexane O…

A: Given :Compound :Objective : To determine IUPAC name .

Q: When an alkene is subjected to treatment with Hg(OAc)​2 in alcohol, followed by reaction with NaBH​…

A: A multiple choice question based on introduction to organic chemistry that is to be accomplished.

Q: Provide the correct IUPAC name for the compound shown here. H₂C. CH3

A:

Q: c) a) C6H5N₂+ b) C6H5CEN rite in the reagent(s) over the arrow. H₂C- CI OH ---→ benzene H₂C…

A: Answer:- This question is answered by using the simple concept of chemical reactions of organic…

Q: Draw the structures of all the possible products that can be obtained from the dehydration of…

A: Alcohol is an organic compound that has OH functional groups.They are reactive due to the presence…

Q: Ethyne and butyne are unsaturated aliphatic hydrocarbons. HCECH HC=CCH,CH3 Butyne Ethyne a) Write…

A: In alkynes  the carbons are sp hybridised due to more percentage of the s character in sp…

Q: Synthesize attached compound from benzene, organic halides with < 5 C's, and any other organic or…

A: Electron withdrawing group are meta-directing. Electron donating group are para- and ortho-…

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: Using chemical equations, show how can you prepare:            3-pentene-1-ol using propyne and…

A: Terminal alkynes are considered to be sufficiently acidic to release H+ ions when treated with…

Q: provide the synthesis of Oleic acid from any straight chain alkanes containing 5 carbons or less.…

A: To synthesis oleic acid from any straight chain Albans containing 5 carbon atoms or less.

Q: e structure of the major organic product of following ring opening rea CH;ONa CH;OH

A:

Q: PQ-2. This reaction is classified as (A) a nucleophilic addition. (C) a nucleophilic substitution.…

A:

Q: Give Introduction about Alcohols, ethers, and epoxides ?

A: About alcohols, ethers, and epoxides are given.

Q: How would you Synthesize each substituient starting with PHENOL. Showing all reagents and…

A: Synthesis for the given compound is as follows

Q: ACCURATE ERRONEOUS IMPOSSIBLE 2,2-dibromo-2,3- nonanediol ethene

A: For the IUPAC name,  rules are there and when these rules are not followed, it will be wrong naming.

Q: D D 6. 3,7-dimethyl-2, 6-octadienal (Citral) till "H + NaBly CH3OH

A: To Draw the products and balance the equation.

Q: The reduction of a certain alkene gave 2-methylbutane. It also gave acetic acid (CH3CO2H) as one of…

A: A question based on alkene that is to be accomplished.

Q: o OH Cyclohexanone, glycers а cro31

A: Secondary alcohol on oxidation with PCC form ketone.  Ketone can then react with 1,2-diol in the…

Q: Draw the organic products formed when cyclopentene is treated with each reagent. With some reagents,…

A: (a) Reduction of alkenes takes place Addition of hydrogen to C-C double bond known as hydrogenation.…

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.