OH H CIe HO, 2.

Q: What is the major product generally formed when a tertiary alkyl bromide  (R3Br) reacts with sodium…

A: the solution are as follows:

Q: РСС, THF 1) NaH Na,Cr,O, 2)CH3CH2CH2BT OH H;0", THF, 25°C PB13 POC13, pyridine, 0°C

A: Cyclopentane contains a ring of five carbon atoms and which group that is alcoholic functional…

Q: a. Write the missing reagents and products. 1. H3O+ 2. tBuOK ? 1. Br2 2. KCN ? ?

A: The given reactions involve alkenes as reactants. In the course of addition to alkene, a carbonation…

Q: Hydration of alkynes is performed in the presence of Hg2+* salts but hydration of alkenes can be…

A: why an acid catalyzed used in hydration of alkenes reaction- Acid catalyzed hydration of alkenes…

Q: Propose a series of reactions that would convert the provided starting material into the given…

A: The question is based on the concept of organic synthesis. We need to synthesize the product using…

Q: How many steps are in a reaction using an organometallic reagent? O 4 O 3 O 2 O 1

A: The reaction of an organometallic reagent with an aldehyde or ketone embodies the most fundamental…

Q: Please Show reaekson and don't use hend raiting

A: Answer((1):To show the acid-base reaction between the given molecule (2-aminoethanol) and sodium…

Q: This is a hydrogenation and carbene addition problem. How do I draw the structure of the major…

A: Interpretation: We have to write the product for the following reaction.

Q: My question is still the same, What is the major substitution product of the reaction, and what is…

A: The replacement of any atom or group of atom by a nucleophile is termed as nucleophilic substitution…

Q: t. solve b and gc

A: Given are organic reactions.The starting compound of reaction b is furan.

Q: What are the steps and reagents used?

A: Applying concept of organic synthesis and reagent.

Q: Categorize the following reaction as an Addition, Elimination, or Substitution. Addition Br…

A: These reaction can be explained as:

Q: Which of the following is aromatic? www www.

A: Aromatic compound which obey 4n+2 rule and it should be cyclic, conjugated and planar.

Q: he reaction of propan-2-ol in the following series of reactions will yield __________. 1)  NaH;…

A: Given  Propan-2-ol 1)  NaH; then set aside until Step 3; 2)  CH4 plus Br2, light and heat, assume…

Q: What are the organic products of these reactions? Are they electrophiles or nucleophiles? What is…

A:

Q: In the reaction (E) 2-methyl -2,4-hexadiene with hydrogen bromide at room temperature, two isomeric…

A: kinetic product form faster and form at low temperature while thermodynamic product form at high…

Q: Predict the products of additions, oxidations, reductions, and cleavages of alkynes, including the…

A: The alkyne molecule has two pi bonds. It acts as an electron-rich source. It undergoes various types…

Q: (a) 2-pentanol Draw the structure of the alkene that was used to prepare the alcohol in highest…

A: Alcohol can be prepared from alkene by hydrating in acidic medium.

Q: Which carbocation would be least stable?

A:

Q: 1 mol NH3 + 1 mol C2H5Cl when heated there is a lot of unreactd NH3 (about 80%). Why does this…

A: When ammonia reacts with ethyl chloride, it undergoes Ammonolysis reaction to form ethyl amine.…

Q: CH3 H3C H30", A H;CH;CO OCH,CH3

A:

Q: Which of the products is the 'E" alkene? Which product is the "Z" alkene? Which product would be…

A: The compound named as A and B for identification so the compound A is 'Z' Alkene and compound B is…

Q: This molecule reacts with HBr to form an alkyl halide. Would this reaction be sn1 or Sn2 and explain…

A: Given : structure of molecule.  Tip : if carbocation is stable then SN1 otherwise SN2

Q: Rank the following alkenes in order of increasing rate of hydrogenation. 11 I < III < IV < || <|| <…

A: 78

Q: The following reaction can produce two products. The first of thes contains ONE double bond. What is…

A:

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.