-CI NH2 R S fID) o (o

Q: Which C-C single bond is strongest? C OA OC D

A: The strong bond or weak bond is considered by its nature. The hybridization of C decides whether the…

Q: Choose a likely identity for X, Y, and Z in these structures. :çi: :-x-: OC Be Be OF F OB ON ON 一一:…

A: In 1st valancy should be 2 to fulfill this formula. So the element X should be Beryllium.

Q: Identify the strongest acid: O о о о H Н H c=c=c I- Н- Н H-CH H Н Н H Н HIC C-H H H Н -H

A: Acidity is defined as the ability of a molecule to release protons. If a compound  easily donate…

Q: Name the following:

A: b. (2S,3S)-2-bromo-3-chloropentane d. (2R,3R)-2,3-dichloropentane

Q: (e) NO₂ CN TI F NO₂ Ph CN

A: For the synthesis of product e  the starting compound is reacted with Base (NaOH) to form a…

Q: (g) 是 N. H₂, Ni

A: In the given example the first reaction is an example of nucleophilic addition reaction of carbonyl…

Q: 64 vo (Acac) E-BUOOH

A: VO(acac)2/t-BuOOH reacts with alkene (its have -OH group at allylic position) and epoxidizes to form…

Q: Give systematic IUPAC names for each of the following: 3 (c) (d) G Br OH (1) Ś Bri Br (g) (h) &

A:

Q: H ΟΞΟ -- H Ο C+ Η

A: A major resonance contributor is one that has the lowest energy. We can often write more than one…

Q: Drawing 1. (CH),CHNH,, No(CN)BH, PH 4-5 2. Neutralizing work-up Atoms, Bonds and Rings tha Charges…

A: Given is organic reaction.The given product is secondary amine.The given reagents are primary amine…

Q: (e) Br- (g)

A: The addition reaction of an alkene with a hydrogen halide to furnish the haloalkane is termed as the…

Q: (е) H H H- C C- NH, H H Br Names:

A: The reaction taking place is given as,

Q: 4-44 Draw the important resonance forms of the following free radicals. (a) CH₂=CH-CH₂ (b) (d) (e)…

A:

Q: OH OH OH H3C,, Br

A:

Q: ✔ L{{{{u++» L][/in.. IV

A: The correct structure of (2S,5R)-2-fluoro-5-methylnonane is

Q: Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the…

A: Alkyl halide undergo dehydrohalogenation in presence of a base either through E1 or E2 mechanism…

Q: Identify A–E.

A: Please find below the reaction taking place

Q: Select the letter which corresponds to the most reasonable mechanism for the Fischer Esterification:…

A:

Q: Solve this queation

A: To solve the given reaction sequence, let's analyze each step carefully, starting from the provided…

Q: Н СНз н н Н-С-с-с-С-С-н H H H CH2H CH3

A:

Q: 1-Methyl-1,3-cyclopentanediol Draw the molecule by placing atoms on the grid and connecting them…

A: 1-Methyl-1,3-cyclopentanediol is a organic molecule with the chemical formula C7H14O2. It is a…

Q: -ОН H-B ути он

A: Here protonation of carbonyl using lewis acid H-B+ to gives protonated carbonyl ,attack of OH lone…

Q: Using curved arrows, show the mechanism for the acid-base reaction. Be sure to show all lone pair…

A: The acid is a species that gives the proton to another species. The base is a species that accepts…

Q: Figure 9-be D A It H H В но P Br кто C(CH3)3 Н с А H

A: In E2 elimination, leaving and beta-H should be anti to each other.

Q: Which is more stable

A: We have given the confirmation of 4-amino cyclohexanol.  The stable confirmation is that which have…

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.