13. For the following reaction, use the identity of the alkyl halide and nucleophile to determine which substitution mechanism occurs. Then determine which solvent affords the faster reaction. OOOO OSN1, CH3OH SN1, DMSO SN2, CH3OH SN2, DMSO CH3OH CH3OH or DMSO OCH 3 HCI

Q: Na O O Na 70NAT +

A: (a)Sodium ethoxide: Sodium ethoxide is used as a base and it will form enolates of esters.

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A: A carbocation is an important reaction intermediate in organic reactions. A less stable carbocation…

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Q: Substitutions of Aromatic Heterocycles DMF POCI3 CH mecanssum mpletely altered by the presence of…

A: In a chemical reaction, the combination of two reactants in an appropriate molar ratio produces the…

Q: A C13H220 |a. BuLi b. O C16H2402

A: First of all we will calculate degree of unsaturation.

Q: CN ΗΝΟ; H2SO4

A: This is an example of nitration reaction

Q: CH3CH₂ONa etanol Br calor

A:

Q: Given the following data: Pals) + 6 Clzig) → 4PC|3(9) AH = -1225.6 kJ Pa(s) + 5 Oz(g) → P4O10/s) AH…

A: enthalpy is an extensive property which will depend on the number of particle.

Q: H₂C I || CH3 CH III 2.0 CH3 IV ppm 1.0 1: 0.91 ppm II: 3.29 ppm III: 3.23 ppm IV: 1.52 ppm C) 1:…

A: We are given the 1H-NMR spectra of a known molecule. We have to annotate the 1H-NMR spectra and…

Q: 13. Suppose the reaction: A + 2B AB2 occurs by the following mechanism: Step 1 A + B → AB slow Step…

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Q: H C H3C CH3 HBr DMSO ?

A: DMSO is dimethyl sulfoximideHBr will be added to DMSO in the given reaction and the formed molecule…

Q: 1s²2s²2p63s²3p64s²3d104p65s²4d4

A: Here we have to predict the symbol of divalent cation of the following given electron configuration.

Q: HO- 나 E1/E2 rcaction

A:

Q: 15. Capillary columns are open tubular columns constructed from which of the following materials? a)…

A: Capillary columns are used in gas chromatography.

Q: The precipitate to be obtained will be more likely colloidal if the computed relative…

A: 25) when the relative supersaturation is large, the precipitate formed likely to be colloidal.

Q: Determine the position that is most likely to be the site of an EAS reaction in the compound below:…

A: Site for an EAS in case of disubstitued benzene is decided as follows:

Q: + PdCl₂

A: A metal with vacant orbitals can readily accept electrons from a donor atom.The donor atom should…

Q: Magnesium bromide, MgBr2, has a lattice energy, AHjattice, of -2406.0 kJ/mol and a heat of…

A: Since you have posted multiple questions, we are entitled to answer the first only.

Q: What is the pressure (in atmospheres) of the gas inside the container connected to an open-end,…

A:

Q: B12 NaOH H₂O NaOCH3 CH₂OH

A: The objective of this question is to predict and apply appropriate reactions and reagents to achieve…

Q: C2 H4 (9) + 302 (g) 2 CO2(g) + 2H2O(1) 2C2 H6 (g) + 702 (9) → 4 CO2(g) + 6H2O(1) 2H2 (g) + O2 (9) →…

A:

Q: N₂03 -> N₂O4 +0₂

A:

Q: H30* `NH3 i) type

A: The given reaction is represented as follows:

Q: g) CH₂CI NaCN CH3CN Δ

A: Information of question

Q: Ag+KNO3

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Q: Which atom is the most nucleophilic? A 0. N N

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Q: Which of the following set of quantum numbers (ordered n, l, m, Ma) are possible for an electron in…

A: The principal quantum number(n) is an integer that is the number of the electron's shell. The value…

Q: The molecule shown below is an inhibitor of the Botulinum neurotoxin. 6 N 5 N -2 S S 3

A: Hybridizationthe concept of mixing two atomic orbitals to give rise to a new type of hybridized…

Q: d. NO₂ H₂ Pd/C

A: H2 in the presence of Pd/C is a reduction catalyst which reduces ketone and nitro groups which are…

Q: 4 CH6 2 NH3 >>

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.