7. Propose methylbutane using water and heat (60°C). a mechanism for the synthesis of 2-methyl, 2-butanol from 2-chloro-2-

Q: 1. (CH3)2NH, H 2. 3. H3O+ A سعید. ملها. B بعد. C D

A: Step 1: Step 2: Step 3: Step 4:

Q: Br NH₂ ΗΝΟΣ H2SO4

A: Nitrous acid is a Bronsted acid of moderate strength. It is unstable and hence, it is prepared…

Q: Which of the following violates the rules for use of curved arrows? III I II IV OI and III II and IV…

A: Violation of rule of resonating structure curved arrows

Q: 4. Identify which of the structures below correspond to a. b. d. e. x CH3CH₂CH₂CH(CH3)2 f.…

A:

Q: The stronger the IMFs the higher the boiling point (a) Draw structures for the two molecules, name…

A: Since you have asked multiple questions we will answer the first one for you. To get the remaining…

Q: Ja

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

Q: Which of the alcohols is 3°? CB 5-од. OH 111 0 A) ОН O B) 0 c) 1 || X. 4 CH, IV -CH₂

A: Since, If carbon containing -OH is surrounded by three carbon then alcohol is known as 3° alcohol.…

Q: (9) NH2 H,C (IC) NH2 HzN

A: 9) The compound given is having 6 carbon cyclic parent chain as shown below.

Q: +2 NH₂

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: O 1) 03 2) (CH3)2S 1) 03 2) Zn, H₂O 1) 03 2) (CH3)2S

A: Alkene reacts with ozone followed by hydrolysis with Zn, H2O or dimethyl sulphur leads to the…

Q: _OH ???

A: alcohols to alkenes in the presence of con.H2SO4 on heating nearly 175oc.

Q: H HH Na Ⓒ HH H Select to Add Arrows NaNHz Na Ⓒ HH Br H Select to Add Arrows

A:

Q: 3) Each molecule below can be altered to form a molecule in the point group listed by removing (at…

A: Point group symmetry

Q: CH₂ HBr H₂O ?

A:

Q: H*, H2O OH

A: Acidic hydrolysis of alkenes involves protonation of alkene to give a carbocation intermediate.…

Q: e. How many T bonds are in the molecule? f. What is the N–N–N bond angle in the azide (–N3) group?…

A: The objective of the question is to solve the given question related to AZT molecule.

Q: There can be more than one correct answer.

A: Cyclohexane is more stable in chair form. Chair to chair interconversion is known as flipping.

Q: xi OH 1) SOCI₂ 2) xs (CH3)2NH

A: The given reaction scheme is shown below.We have to give the product of the above reaction.

Q: KO KO KO Select to Add Arrows Select to Add Arrows

A:

Q: !!! Question 2 Not yet answered Marked out of 6.00 Flag question a) C,HJNH, + H,O → C,H,NH5 + OH-…

A: First, we need to identify the type of reaction for each equation. The reactions can be classified…

Q: What is the nlx notation of 81Tl

A: The given element is 81Tl.

Q: H₂O, HCI (cat) CH3OH, HCl(cat) O OCH3 HOH H HO O CH3CH2OH, HCI (cat) HO H -OCH2CH3 OHI H H

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

Q: 3. Titan Life? Let's now think about the possibility of life on Titan (a moon of Saturn), which has…

A: Phospholipids are a type of lipid molecule that plays a crucial role in the structure and function…

Q: help q9

A:

Q: H H A HB Н B CH3

A: a. This is a bicyclic compound with a ketone group at the 2-position. The system is…

Q: Which of the following structures is consistent with the IR spectra shown below? % Transmittance 80…

A:

Q: Practice Problems: H3C- -c-o- -о—н CI

A: Alkene gives epoxidation reaction with peracetic acid or meta-chloroperbenzoic acid. The reaction…

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.