Which of the following bases would you not use to deprotonate 1- pentyne? B H3C H3C CH2 lithium n-butyllithium lithium methoxide dimethylamide lithium methoxide O n-butyllithium lithium dimethylamide

Q: What types of reactions are taking place and the correct starting compounds. Me3SICI, Imidazole…

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

Q: What sort of reaction is shown below? OH Reduction Acid-Base Esterification Addition Elimination…

A: The reaction between an acid and a base to give salt and water is called neutralization reaction.…

Q: QUESTION 10 Which functional group consists of four atoms? ketone ester carboxylic acid aldehyde…

A:

Q: Identity the Aldehydes or Ketones from an Acetal or Hemiacetal OH OH OH OH 0- H Aldehydes Ketones

A: Aldehyde or ketone reacts with alcohol gives acetal

Q: Name the class of compound: 0 CH3CH2CH2CH Alcohol Aldehyde Carboxylic Acid Ester Ether Ketone

A: Given,The compound is:

Q: OH (1) OsO4 (1) mCРBА CH3 H3C (2) NaOH H20 (2) NaHSO3 OH

A:

Q: он + Na OH + Na CI

A:

Q: What is the IUPAC name of the following compound? Ph HO. O 5-methyl-5-phenylhexanoic acid O…

A: Option A. 5-methyl-5-phenyl hexanoic acid

Q: What types of reactions are taking place and the correct starting compounds. Me3SICI, Imidazole…

A: The question is asking about the types of reactions that are taking place and the correct starting…

Q: Draw the organic product(s) of the following reaction. Aqueous H2SO4 H2N-N- + ethanol

A: Solution ;      Fischer indole synthesis: This reaction is one of the types of pericyclic…

Q: Complete the following reaction scheme. Keep in mind that the sequence starts with an alkene or…

A:

Q: butanoic acid+NH3

A: When carboxylic acid is made to react with ammonia,it results into the formation of carbamide with…

Q: Draw the product(s) formed by heating the compound shown in acidic methanol. CH3OH H* heat

A: This is trans esterification. CH3OH is work as a nucleophile.

Q: When aniline undergoes addition to an electrophile, the carbocation intermediate has a variety of…

A: In the electrophilic aromatic substitution of benzene derivatives, the substitution of incoming…

Q: Draw the organic product you would expect to isolate from the nucleophilic substitution reaction…

A: Step 1: Step 2: Step 3: Step 4:

Q: Draw the organic product you would expect to isolate from the nucleophilic substitution reaction…

A: There are two reactants: a tertiary alkyl iodide and water . In the substitution reaction, water…

Q: Which of the following functional groups can be found in trans-Cinnamic acid? Group of answer…

A: The compound considered is trans-Cinnamic acid.

Q: H. H H- С—с H H H Name the following aldehydes hello. ÇI H CH, O 41 31 21 ; Н-С-С-С-С-Н H H CH, OH н…

A: ALKANAL

Q: What is the correct name for this compound?

A: IUPAC nomenclature of aldehyde: • Identify the longest continuous carbon chain. • Identify the…

Q: CH3 НО ОН CH3 H Cortisol a) NaCN b) H3PO4 85% c) NABH4 .. I sבוווי

A: The question is based on the concept of organic reactions. we have to identify which of the…

Q: aldehydes and ketones 1 Which of the following statements about the reaction of aldehydes and…

A: option (c) is correct . Aldehyde when undergoes oxidation reaction in presence of acidified…

Q: 3. Which three of the following carbonyl compounds would most likely form a stable hydrate? A A. B.…

A: # For the formation of hydrate from a carbonyl compound, it depends on two things, first, the…

Q: Which of the following functional groups are present in decanedioic acid? Group of answer choices

A: Functional groups are the substituents which are directly attached to the alkyl chains of…

Q: What types of reactions are taking place and the correct starting compounds. Me3SICI, Imidazole…

A: The question is asking about the types of reactions that are taking place and the correct starting…

Q: What types of reactions are taking place and the correct starting compounds. Me3SICI, Imidazole…

A: The question is asking about the types of reactions that are taking place and the correct starting…

Q: If the enolate forms at carbon 1 and then reacts with the carbonyl carbon 5, what size ring product…

A: Organic compounds are mostly made up of carbon, hydrogen, oxygen and nitrogen atoms, and organic…

Q: ? H₂N N=

A: A series of reaction required to get the product.

Q: Which of these 5 compounds is likely to smell best? Write that answer first. Then, which of the 5 is…

A: The smell of organic compounds can be generally attributed to the functional group present in the…

Q: How could one convert an aldehyde to a carboxylic acid? Group of answer choices-   Reduce the…

A:

Q: + 2 + 2 H2 H2 N ОН -ОН Pt Pt H+ H+

A: We know that H2/Pd is a reducing agent. The aldehyde group is reduced by the H2/Pd to form a primary…

Q: What is the IUPAC name of the following compound? NO2 Br COH O 2-nitro-6-carboxybromobenzene O…

A:

Q: Which is the major product from the reaction of propene with BH3 followed by NaOH/H202? a)…

A:

Q: Look at the atom in each molecule and classify as an electrophile or a nucleophile. How do you know…

A: Electrophiles are those species which are deficient in electron. While nucleophiles are those…

Q: What is the systematic IUPAC name for the following Organic compound? مند O Hexanoyl chloride…

A: Naming of Acyl halide: With the name of the parent chain add 'oyl' followed by the halide name.

Q: For the following syntheses, determine what reactions are needed to form the given products. но HO…

A: The question is based on the concept of organic reactions. we have to convert the given reactant…

Q: ОН CH3 HO, OH CH3 H. Cortisol a) NaCN b) НзРО4 85% с) NaBH4 d) NaH е) NaOH

A: To check which reagent attack which functional group

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.