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Q: 18. Name the following compounds. Make sure to include the R/S designation. CH₂ 있으 원

A: Basic rules for IUPAC nomenclature:1) Select longest chain or block of carbon atoms as parent. 2)…

Q: The decalinols A and B can be equilibrated using aluminum isopropoxide in 2-propanol (isopropyl…

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Q: ☐ อ コ コ HO O H2SO4 XS xs H₂O Click and drag to start drawing a structure.

A: Product of following reaction can be made by applying appropriate reaction mechanism.

Q: 1. Fill in the appropriate reactant or product as necessary. 2-フーフ フー3-3-つ olf b. (-C=C-C

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Q: Q2 | Prepare the following Compounds ? 1-Asprin 2-Acetanilide 3-Phenol

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Q: draw curly arrow for below mechanisem

A: The reaction may follow the below predicted mechanism as the amine group will act as nucleophiles…

Q: Be sure to answer all parts. Give the IUPAC name for the following compound: O CH₂CH3 CH3CCH₂CCH₂CH3…

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Q: -COH (acid) &H (aldehyde) Ar-H (aromatic) (C-C-H, vinylic OH (alcohol or phenol) X-C-H (X= halogen…

A: The 1H NMR spectrum given contains two peaks indicating two different proton environments.

Q: What is the major product of the following reactions? 1) LDA -78°C OCH, 2)

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Q: 102 100- 95 733.63cm-1, 96.21%T 90 1167.81h-l 92.47%T 69.96cm-1, 93.62%T 10 04cm-1, 89.79%T 85 28H…

A: On deciding the structure of an unknown compound, the preliminary information about the compound…

Q: For each solute, click the button under the better solvent. :0: solute HO-C-CH-CH₂-C-OH OH :0: :0:…

A: Like dissolves like principle states that polar compounds are soluble in polar solvent and non-polar…

Q: HCI не Par

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Q: Predict the major products of the following organic reaction: id. I Some important Notes: .Draw the…

A: This is an example of Diels-Alder reaction. It is a pericyclic reaction which involves…

Q: What is the structure for this compound? 3-sec-butylpyridine Please explain your reasoning. Thank…

A: 3-Butylpyridine belongs to the class of organic compounds known as pyridines and derivatives.

Q: Click the "draw structure" button to launch the drawing utility. Draw the product of the following…

A: Lithium aluminium hydride, LiAlH4  is a powerful reducing agent commonly used in organic synthesis…

Q: Provide the correct IUPAC name for the compound shown here.

A: Since,Rule of IUPAC-1) Longest chain as parent chain.2) Numbering start from those side where more…

Q: Part A Indicate if each of the following is soluble in water. Drag the appropriate compounds to…

A: Amines are soluble in water because of their ability to make Hydrogen bond with water molecules.

Q: What is the IUPAC name for the following compound? CH₂=CH-CH=CH-CH=CH-CH₂-CH3

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Q: draw out a step by step mechansim with arrows to get from the compound on the lefts to get the…

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Q: show-all-working-explaining-detailly-each-step Answer should be typewritten with a computer

A: A option is correct.  Phenylethanal It can't be option B and C because of molecular formula and in D…

Q: Give the major organic product(s). 1. H3C HO H₂C НО CH₂ CH CH₂CH₂ CH₂O MgBr CH₂ CECH S=C Na…

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Q: A. What is the cell notation of the set-up? B. What is the standard cell potential (Eºcell)? C. If…

A: #B: Since Au has a higher reduction potential, Au3+(aq) undergoes reduction to Au(s) nad Ni(s)…

Q: Please don't provide handwritten solution .....

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Q: 2. Draw structures for the following systems. If more than one isomer is possible, draw strcutures…

A: Isomers have same molecular formula but different structures.

Q: N CH3 gogo N N-O F Risperidone (Final Product)

A: Here we have to identify and circle all the functional groups and write their name and identify the…

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Q: What is the IUPAC name for the molecule shown? CI O…

A: Nomenclature of organic compounds.

Q: thank you 3. Name each of the following carboxylic acids, using the I.U.P.A.C. Nomenclature System:…

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Q: Click the "draw structure" button to launch the drawing utility. The following reaction has been…

A: Nitriles after complete hydrolysis under acidic condition give carboxylic acid

Q: ーンフーク 27.

A: Here we have to synthesize the following given target compound from the starting materia 1-methyl…

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A: Alcohol - aliphatic hydroxy compound Phenol- aromatic hydroxy compound

Q: C. d. Br l CH3OH NaOCH3

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Q: help please answer in text form with proper workings and explanation for each and every part and…

A: Step 1: Nitration of BenzeneC6​H6​ + HNO3 ​  →  H2​SO4​  →   ​​C6​H5​NO2​ + H2​O     Step 2:…

Q: Which will not produce a green flame? * Bromoform Thioformaldehyde chloroform Carbon tetrachloride…

A: A. Beilstein test is used to detect the presence of halides. A Cu wire is heated strongly to get a…

Q: 1. Show how you would synthesize each compound from starting materials containing no more than six…

A: In the synthesis of the first compound the reaction of benzene with acid chloride and AlCl3 is…

Q: 3 PPM 2 180 El-MS: 88.1 160 140 120 100 PPM 80 60 40 20 0

A: Number of signals in 1H NMR = Number of sets of protons in different electronic environment Position…

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A: Step 1:• In this reaction, Firstly base abstract the acidic proton to forms enolate ion which…

Q: CH-CH-NH-CH, [ Select ) H3C-N CH3 | Select] NH, v ( Select ] H,C. NH 1,4-diaminohexane…

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Q: Provide an IUPAC name for the compound below. B sure to specify stereochemistry, (E) or (Z), where…

A: The IUPAC (International Union of Pure and Applied Chemistry) nomenclature is a widely accepted…

Q: Can someone please answer E-H! thank you

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Q: What is the pH of the sodium lactate solution? C3H5O3 + H₂O = HC3H5O3 + OH- [C3H5O3] = 3.22 × 10-¹ M…

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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.