match with following: LiCI with water C8H18 with itself SO2 with itself CH3OH with itself CF4 with itself Strongest IM attraction 2nd strongest IM attraction 3rd strongest IM attraction 4th strongest IM attraction 5th strongest (weakest) IM attraction

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: Which molecules shown will form strong hydrogen bonds with water?

A: Hydrogen bond: hydrogen bond is defined as the electrostatic attraction between the positively…

Q: CHO O CNHET

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: (H) = Na2CO3' H₂O

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Q: A 0 ΝΗ B NH

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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: Classify the following alcohol molecules: Compound I is compound Il is V. compound Il is v and…

A: The given alcohol molecules are to be classified into primary, secondary, and tertiary alcohols.…

Q: HN' CH3 C A

A: The hydrolysis of ester, amide and acyl chlorides depends on the tendency of how strong the leaving…

Q: Provide the intermediates and/or reagents needed to complete this synthesis.. Ignore inorganic…

A: For the above given reaction sequence the intermediates formed and the reagents used are explained…

Q: Indinavir (trade name Crixivan) is a drug used to treat HIV. Question: At which sites can indinavir…

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Q: Find

A: NaOH act as a Strong Base. because of its OH(-) ion abstract H(+) ion from the phenolic OH group and…

Q: Hydrogen bonding between amide molecules may be shown as in O CH-C-N-H --- H-N-C-CH, H H CH3-C-N-H…

A:

Q: HO TpH OH OH + NaOH (1 equiv) va plC2-9.782 charge pH 11

A: Carboxylic acid reacts with NaOH to form sodium carboxylate.Phenol reacts with NaOH to form sodium…

Q: PartA What is Iho balancod chemkalequaton tor the roacton used e cokuato AF; SrCOs(e)? i ucieral…

A: The given compound is SrCO3(s).

Q: CH OH What type of compound is the following? O 1º alcohol O 2º alcohol O 3º alcohol O phenol

A: It is 3o alcohol as all H atoms are substituted with the groups.

Q: wrire disociation re action for rhe moleculo Sand abel comnj ugate acid base pairs CACA,(0o4,…

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A: Step 1: Step 2: Step 3: Step 4:

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

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Q: (4) он LIAIH4 он NaBH4 NaH

A: Chemical reaction:

Q: PLease draw the Follocoing stueture in the most 8table chair fom.sustily youm chotee

A: While placing the position of substituents in the chair form of cyclohexane, pay attention at the…

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A: Answer image:Step 1:Given that,The Lewis structure of the pentane shown in the question.The…

Q: (Q62) If strong acid is added to a solution containing calcium carbonate, what species will form in…

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Q: B H for each compound circle each atom to that could hidrogen bond with water A H ---- H-C с 1 H H H…

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

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Q: Solve this queation

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

Q: None

A: Step 1: Rule for Naming(I) Select the longest carbon chain(II) Start the numbering from of carbon…

Q: Which of the following compounds contains both a hydrogen-bond donor and a hydrogen- bond acceptor?…

A: For any molecule to make hydrogen bond with another molecule, it should be either a hydrogen bond…

Q: CH,OH он H он H он H CH,OH H. OH H он H H OH

A: Given structure is : What type of glycosidic bond is here = ?

Q: از m) es OH CH 3 Br I X J он 2CH3 + HBr + Nal OH

A: The answer to the following question is-

Q: A common ketone starting material is shown below. Predict the major product for each reaction based…

A: Ketones are potential functional groups from that we can prepare different functional groups.

Q: Use curved arrows to show the flow of elections on the reactant side of each of the following…

A: Given  (a)  Ketone and OH- reaction        Curved arrow mechanism (b) reaction of Alcohol with HCl…

Q: The amine shown can be classified as O 1° 2° 3º O aryl .OH

A: Amines are classified into four different classes. Those are discussed belowPrimary amine (1°):…

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.