ASAP!!  and change 2pentane to 2 -pentanone !! Thanks

Q: 19. Which of the following compounds will undergo oxidation using potassium dichromate to form a…

A: Alcohol undergo oxidation to give aldehyde, carboxylic acid and ketone. Primary alcohol undergo…

Q: What is the correct IUPAC name of an Ester below? * H3C CH3 Butyl pentanoate Pentyl butanoate Butyl…

A:

Q: SOCI, HO, of ELOH of Cl, NaOH H,O/dioxane

A: The Question  is based on the concept of organic reactions. We have to identify the reaction and…

Q: Br 1. NaOCzHg, CzH,он 2. NaOH, H2O 3. Н,о", һeat

A:

Q: NH2 H3C CH, но H,N., A NH2 6 M H,SO, H3C. H,C H3C. H,C HO, H,C CH, CH CH NaOAc…

A:

Q: A. Provide IUPAC names for the given structures or structures for the given names.…

A: All these given compounds are examples of different amines with various substituents at different…

Q: Q5:- Give structures and names of the principal organic reactants and products of the following…

A:

Q: how to convert 1-butanol into 4-heptanol

A: Try read more about the reaction of the given

Q: How can I make 2-pentanone out of n-butanol?

A:

Q: ▷ 8. acetophenone + NaBHY CH₂OH

A: To draw the products and balance the equation.

Q: butylpropylamine Express your answer as a condensed structural formula. Do not include bonds between…

A: The given compound is an example of secondary amine with propyl and butyl substituents.

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.