1. Anti-aromatic compounds are planer and follow the 4n pi-electron rule. True or False 2. lons can be aromatic. True or False

Q: Which of the following substrates CANNOT be cleaved using periodic acid? ОН s OH 수 OH

A: The above all the substrates are Vicinal diols . When the Vicinal diols react with the periodic acid…

Q: OM OM Heat NOE! H

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Q: IUPAC name Please....

A: IUPAC nomenclature rules for alkenes and alkynes: • Identify the longest continuous carbon chain. •…

Q: BF3 ? + + : NH3 ? ? + NH3 : CI:

A: 1. Arrhenius Acid: An Arrhenius acid is a substance that, when dissolved in water, increases the…

Q: Name the following compounds using IUPAC conventions .CH3 O₂N OCH3 CI CH3 CH3 CH3 CH3

A: Rules for IUPAC naming:- Select the longest chain which contains carbon-carbon single bonds.  Given…

Q: ive detailed Solution with explanation needed

A: Addition of electrophile to unsymmetrical alkene is regioselective. It takes place according to…

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

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Q: ▾ Part C Name the following compound. CH3 CH₂-CH-CH₂- Spell out the full name of the compound. ▾…

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Q: vide the correct common name for the compound shown here. CH3-CH2-CH2-CH₂-CH₂-O-CH₂-CH₂-CH₂-CH3

A: IUPAC nomenclature is used for naming the organic compound as recommended by international union of…

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Q: エ。 10 エ エ エ エ

A: A carbon can only make 4 bonds as its valency is 4 so we will use hydrogen bonds accordingly. Lone…

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A: The given 3D molecular structure of monosodium glutamate molecules.Sodium atom --> purple…

Q: :ö-H....ö-H H

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Q: D H3C D CH3 H₂ Pd, Al2O3. CH.CO2H

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

Q: What is the number. the following of molecule? NH & bonds.

A: Since, In the molecule, single bond known as sigma bond. If double bond is present in it contain one…

Q: 3) Which regresents the eno form of the following molecule?

A: Keto enol tautomerism is a type of structural isomerism. A chemical equilibrium between the keto and…

Q: Physical state of hexane

A: The Physical State of hexane is Liquid.

Q: The invisible field surrounding all magnets of other magnets. O a magnetic field south pole O c…

A: The invisible area around a magnetic object that can pull another magnetic object toward it or push…

Q: B) HHH I H-C-C-C HHH H H-C-H H-C-O-H H The functional group is... H The class of molecules is... H…

A: The given compounds have individual functional groups which provide special characteristics to the…

Q: CHy-L LIAIH, nBu-Li CHO ÓMOM LIAIH

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Q: 159 253 74 Ge → To Cf 98 +. 65 32

A: Total atomic number in reactant side 98+32=130 It should be balance 130=65+X X= 65 Total mass in…

Q: first. CHg +O2

A: Combustion is commonly called burning and the substance that burns is usually referred to as fuel…

Q: 3. It is required to introduce a halogen group to a five membered ring, thiophene. Discuss the…

A: When an atom of a cyclic hydrocarbon is replaced by a heteroatom such as nitrogen, oxygen, and…

Q: What is the common name of the following compound? CH3 CH3CH₂CHOCH3

A: This problem is based on general organic chemistry and its nomenclature. The solution is given…

Q: Determine whether each of the following molecules can exist as cis-trans. a. 1-pentene b.…

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Q: Draw structures to explain ring-flipping. Be sure to show all hydrogens. 1 Describe the positions of…

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A: For IUPAC naming of ester -> Identify the longest carbon chain containing the carbonyl…

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A: Recall the given reaction,                              5 CaOH2 aq  +  PO43- aq  →  Ca5OHPO43 s  +…

Q: 7. Which functional group is not present in the molecule illustrated below? A. Aldehyde B. Ketone C.…

A: A) Aldehyde (-CHO): in this the carbonyl group (C=O) is present in one of the terminal of the…

Q: Br + HNO; and H2SO4

A: Since you have posted multiple independent questions in the same request, we will solve the first…

Q: Question attached

A: Dipole moment is  VECTOR quantity. It is equal to the product of charges and distance between them.…

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Q: Which molecule has the lowest boiling point

A: Alcohol and carboxylic acid show greater extent of H-bonding. They has definitely higher boiling…

Q: 3D model Formula Name ion ball & stick + labels ion ball & stick 1-1+ labels ion

A: 1. General formula of this structure should be M(A4B2)2- and ion is anion.

Q: Please correct answer and don't use hand rating

A: Step 1: Dissolution in water. When we have a mixture of two substances, such as sodium thiosulfate…

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A: Dispersion force is weakest intermolecular force and this intermolecular force exists between all…

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Q: Provide the correct common name for the compound shown here. ..||||

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Q: Name the following compound & ****** Spell out the full name of the compound. Name the following…

A: If the two functional groups are on the same side of the plane, then it is considered "cis". If the…

Q: Which resonance structure results when the electrons are moved according to the curved arrow shown?…

A: When electrons are moved according to the curved arrow, the lone pair of electrons on the…

Q: 7. Entropy changes cannot be measured with a calorimeter like enthalpy changes. If the result upon…

A: ENTROPY: It is a thermodynamic property which is a measure of disorderliness or randomness of a…

Q: H,C, CH3 H,N°

A: iupac nomenclature is accepted worldwide for the naming of organic compounds.

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.