Indicate the major organic product from the reaction shown. CuLi Br

Q: - Reaction of methyl 4-fluoro-3-nitrobenzoate with morpholine LOCH3 NH ? F NO₂ MeOH

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Q: 2. Predict the 'H NMR spectrum of the following molecule and indicate the number of hydrogens that…

A: Nuclear magnetic reasonace is a technique that is used to predict the structural formula of the…

Q: [H*] HO H ELOH [H*] HO H. H20 OH

A: The detail explanation of the organic reactions are given below

Q: Is this the correct way that the mechanism works?

A: Structure of indole is given below.

Q: Can you explain it ? And the mechanism

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Q: H,SO, + CH3CHO NH2 NH ČH3

A: At first the carbonyl oxygen undergo protonation to increase the electrophilicity of carbonyl group.…

Q: 1. LAH 2. Hyo® f. Et Me

A: LAH is Lithium aluminum hydride. it can give hydride ion which acts as a nucleophile. Reduction of…

Q: Substance Water, H₂O Ammonium Nitrate, NH4NO3(s) Aqueous Ammonium Nitrate, NH4NO3(aq) Nitric Acid,…

A: Given,  The incomplete reaction: NaOH + HCl →

Q: Indicate the major organic product from the reaction shown. 1. Li 2. B(OCH3)3 Br 3. Pd(PPH3)4 NaOH…

A: This is an example of cross coupling reaction. It involves four steps.  A. Oxidative addition.  B.…

Q: 2. Predict either the reagents, products, or starting materials for each reaction. Some of these may…

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Q: 1. CH3M9BR 2. H30+

A: Grignard reagents are commonly written as RMgX where R is the alkyl group and the X is the halogen.…

Q: What is the major product of the following reaction sequence? H*, CH;OH

A: Epoxides are cyclic ethers with three membered ring containing oxygen atom. These can open up in…

Q: Diagram the mechanism of the reaction and draw the product(s): Br + AIBT3

A: This reaction is electrophilic substitution..

Q: 2. Rank the indicated protons by increase in acidity (from the least to the most acidic). For full…

A: In order to solve this question, we will form the conjugate bases in each case and see where the…

Q: The following reaction scheme involves different types of reaction mechanism to produce various…

A: a. Haloalkanes are compound having halogens , that is chlorine , bromine , fluorine and iodine…

Q: Nal + F,

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Q: What starting material would produce the polymer shown? Grubbs' catalyst in

A: Grubbs catalyst react with olefin gives cyclobutane type molecule. Which breaks into olefin and…

Q: CH;CHO/HCI 2 N. Ph CH3

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Q: OH Pi ÓH Но OH

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Q: Is this reaction mechanism correct?

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Q: In halogenation of alkane, the HBr gas would evolve to have a positive reaction?

A: In halogenation of alkane, the HBr gas would evolve to have a positive reaction? Explanation of the…

Q: The rate law for the reaction of NO with Cl2 was found to be 2 NOg) + Cl2e) → 2 NOClg) Rate= k[NO]?…

A: Rate law For a reaction, aA+bB→cC+dD Rate can be written as; rate=k [A]a[B]b [A]=concentration of…

Q: Ме Ме Ph Me H* -Me -Ph

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Q: Cl2 H20 ÇN „NH2

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Q: Indicate the major organic product from the reaction shown. Br CN Pd(OAc)2 P(o-tolyl)3 (CH3CH2N

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Q: Indicate the major organic product from the reaction shown. Grubb's catalyst 2.

A: Grubbs catalyst is,

Q: average cycle time with the doubled KBrO3 concentration is 40 and average cycle time with initial…

A: Given data: Average cycle time with the doubled KBrO3 concentration = 40 Average cycle time with…

Q: Determine the four-indices and three-indices Miller-Bravais directions shown below for the hexagonal…

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Q: e,f,g

A: Electron affinity is the amount of energy released when a neutral atom accepts the electrons to…

Q: HÖ: H,O + CH3OH OCH3 :0: : :

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Q: When elements are arranged by increasing atomic number, and by periods according to their…

A: According to the given question we have, as we move across the period the atomic number increases.…

Q: a. b. NaOCH₂CH3 1) LDA, RT 2) CH3CH₂Br

A: An enolate is an anion formed by deprotonation of a carbonyl compound, typically a ketone or…

Q: In a reaction between butyl chloride, C,H,CI(aq), and water, the concentration of butyl chloride is…

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Q: Lewis acid produce cyclooligomerization + BF3 Q-BF3 +2 0 0

A: Lewis acids are those molecules which can gain a pair of electron.

Q: a) Predict the major products when (E)-2,5-dimethylhex-3-ene is treated with Br2 and irradiated with…

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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.