+Br2 Br2 in H2O 1. O3 2. Me2S НаPd 1. Hg(OAc)2 in THF/water 2. NaBH4, NaOH 1. ВН-THF 2. HО, NaOH peroxyacid HЕr HBг(peroxide 1. OsO4 2. NaHSO3

Q: (RI-Limonene is found in many citrus frults, Including oranges and lemons. Which structure is the…

A: Enantiomers which has non superimposible mirror image relationship.

Q: Hyaluronic acid, a component of connective tissue, is the fluid that lubricates joints. It is a…

A: The general structure of hyaluronic acid is as follows,

Q: Atorvastatin (Lipitor) is used to decrease patient serum cholesterol levels. It works by inhibiting…

A:

Q: What product is formed when D-Altrose is treated with C6H5CH2NH2, mild H+

A: An imine is formed when an aldehyde or ketone reacts with a primary amine. The reaction is catalyzed…

Q: Give the structure corresponding to the following name. trans-2-ethynylcyclopentanol

A: trans-2-ethynylcyclopentanol is a cyclic compound which consists of five membered saturated ring and…

Q: Which compound would be most reactive toward autooxidation? о

A:

Q: Draw the following sugar derivatives. ) 2,3,4,6-tetra-O-methyl-d-mannopyranose(

A: The given sugar derivatives can be drawn as  2,3,4,6-tetra-O-methyl-d-mannopyranose

Q: One step in the gluconeogenesis pathway for the biosynthesis of glucose is the partial reduction of…

A:

Q: Draw the most stable chair conformation of β-D-galactopyranose. Name and draw the major product that…

A: We have to draw the most stable chair conformer of β-D-galactopyranose.

Q: What product is formed when attached compound undergoes anintramolecular reaction in the presence of…

A: From the given molecule Initially mechanism is shown followed by the product is given as follows

Q: chloride

A: Dear student this question is related to organic chemistry.

Q: Draw the products formed when D-altrose is treated with below reagent [1] NaCN, HCl; [2] H2,…

A: By adding one carbon to the aldehyde end of an aldose, Kiliani-Fischer synthesis lengthens a…

Q: What products would be formed if CH3CH2CHOHCH(CH3)2 is dehydrated?

A:

Q: Draw the structure of 5-methylhexanoic acid; d-methylcaproic acid:

A: The given organic compound is 5-methylhexanoic acid or δ-methylcaproic acid. The presence of the…

Q: Draw the products formed when α-D-gulose is treated with below reagent Ac2O, pyridine

A:

Q: Draw the structure corresponding to following name. sodium α-bromobutyrate

A: Salts of carboxylic acids can be named by writing the cation name followed by the name of acid with…

Q: The most stable conformation of the pyranose ring of most Daldohexosesplaces the largest group,…

A: For D-idose, the two possible chair conformation of α and β anomer are drawn as,

Q: Classify attached substituent as electron donating or electron withdrawing.

A: Organic reactions are carried out in presence of reactive groups. Some of them are electron donating…

Q: Draw all possible constitutional isomers of a triacylglycerol formed from one mole each of palmitic,…

A: Triacylglycerols (triglycerides) are the lipids formed by the reaction of glycerol and fatty acids.

Q: Interesterification of two mono-acid triacylclycerols gives, in principle, 8 different kinds of…

A: Please find your solution below : Transesterification reaction is the process of exchanging the…

Q: Define the Stereochemistry of Epoxidation ?

A: Epoxidation is a process of converting C=C into epoxides (or oxiranes). It is a single step reaction…

Q: Complete the following Fischer esterification reaction

A: Complete the following Fischer esterification reaction

Q: Draw the products formed (including stereoisomers) when attached compound is reduced with NaBH4 in…

A: The given compound is,

Q: Answer: Answer: Answer:

A: Z isomer is assigned when the highest priority groups are on the same side of the double bond and E…

Q: Draw the organic products formed in each reaction.

A: The starting reactant is valine which is an amino acid. This was treated with acetic anhydride and…

Q: draw the enantiomers' and diastereomers of the following compunds.

A: 1. hexene2. butene3. butyne4.  pent-2-yne

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.