Which of the following is best set of conditions for the preparation of tert-Butanol? 1-tert-butyl fluoride in water 2-tert-butyl bromide and NaOH in DMSO 3-tert-butyl bromide in water 4-tert-butyl fluoride and NaOH in DMSO

Q: Write the appropriate reagents and products for each of the following reactions: HO CH3 HCI (2) ?…

A:

Q: OH

A: IMPORTANT POINTS:   BENZENE is converted to benzaldehyde by gatterman koch synthesis, in this…

Q: Explain why the ortho-substituted 2-nitrophenol in 30-40% yield and the para-substituted…

A: Intramolecular H-bonding: It is present within the molecule.Intermolecular H-bonding: It is present…

Q: Which of the following compounds will dissolve in aqueous NaOH after undergoing reaction with…

A: We have to predict the compound that can be dissolved in NaOH.

Q: most reactive with H20 acting as a nucleophile or base? 4-bromo-1-pentene 3-bromo-1-pentene…

A:

Q: Equivalence point pH = Use correct number of significant digits;

A: The pH scale is introduced by the scientist Sorensen in order to express the H3O+ ion concentration…

Q: How many of the following compounds are suitable for conversion to a Grignard reagent? 00 01 Br 02…

A: Grignard reagents react with alcohol group (-OH), aldehyde group (-CHO), keto group (R-CO-R).

Q: Write all steps involved in the formation of the three products of the following transformations. 1.…

A: The question is based on organic reactions.We need to identify the product and explain its…

Q: p-toi chloride Nal HO pyridine acetone

A: Applying concept of organic synthesis and reagent.

Q: What is a good reagent to oxidize primary alcohols to aldehydes? Sodium borohydride Potassium…

A: Given options are : a). Sodium borohydride b). Potassium permanganate c). Pyridinium chlorochromate…

Q: Consider the diagnostic tests used in CHM 126 to detect the presence of a particular functional…

A:

Q: 10. How many electrons are transferred in this reaction? From which element to which element?…

A:

Q: Write the appropriate reagents and products for each of the following reactions: ? ОН

A: Here we have to use dehydrating reagent to form the given product. We can use reagents such as- 1)…

Q: Provide reasonable starting materials for the following reagents and products. PBr3 Br₂ NaOH Br Br

A: In these two questions we will draw the structure of the starting material from the given reagents…

Q: Br2, H3O+ གོ་ཤི་ན་ཤི་ H3C CH3 CH3 CH3 Aldehydes and ketones can be halogenated at their a-position…

A: Please see attachment below for curved arrow mechanism.Explanation:Step 1: Step 2: Step 3: Step 4:

Q: Acid catalyzed dehydration reaction of 2-methyl-1-butanol produces 2-methyl-2-butene as the major…

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

Q: What is the reagent for the following reaction? NHANH, KOH

A:

Q: What is the major organic product obtained from the following sequence of reactions?

A: To solve this problem we have to know about SN2 reaction i.e bimolecular nucleophilic substitution…

Q: لمد HO HO.

A:

Q: Be sure to answer all parts. Synthesis of the following compound can be accomplished using…

A: We have to draw the product for part 3 and part 4 of the given reaction steps.

Q: Which of the following is produced when an epoxide is reacted with aqueous hydrochloric acid?…

A:

Q: What is the major organic product obtained from the following reaction? OH 3 2 OH

A: Given reaction:we have to find the major product

Q: CH3 CH3-CECH CH3-C-CH3 CH3-0-CH3 EN: I II III IV

A: Electrophiles have  low electron density while nucleophiles have high Electron Density.

Q: Phenol when treated with excess of bromine carbon disulfide gives a product of *…

A: We have given that  Phenol when treated with excess of bromine carbon disulfide gives a   We have to…

Q: Provide the appropriate reagents or product in the following examples.

A: Given ; reactant

Q: 850 What is a [OH-] = 3.4×10²³m? the pH of a solution that contains a [

A: Given that, [OH-] =3.4×10-5 M Then, pH = ?

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: Which compound is an alcohol that may be oxidized to a carboxylic acid by Na2Cr2O7/H2SO4? Of the…

A: The question has three sub parts  which are solved below.

Q: chemical (Electrophilic aromatic substitution) reactions of the Phenol namely; Halogenation…

A: The answer is given as follows

Q: он OH OH он OCH3 CI CH3 10.0 10.2 9.2 7.7

A: Give an explanation, why the acidity of these phenolic derivatives give these pKa value?

Q: Select the reagents that will allow the following transformation(s) to occur. -H ? 1) NaOH 2) propyl…

A: The transformation reaction from propyne (also known as methyl acetylene) to hex-2-yne involves…

Q: NH2 C- C1 A H C- C2 H B1 ČI B2 CI

A: Note: Since, we solve upto three parts, the solution of first three parts are solved below. (a) The…

Q: Other than the aromatic ring, what functional group is present in the major organic product of the…

A: The reactant undergoing oxidation in presence of KMnO4/H2O is n-butylbenzene.

Q: Which of the following is the product in this Grignard reaction? OH O 1) O 2) O 3) ОН 4) H.

A: Need to draw product of the given reaction.

Q: Which of the following compounds are suitable solvents for Grignard reactions? 1,4-dioxane

A: 1,4-dioxane compound is suitable for Grignard reaction.

Q: What are the reagents/conditions needed for these transformations?

A: The condition needed for the above transformation is given in attached image.

Q: None

A: Step 1:Acetal formationAcetals are generally formed during the interaction of a carbonyl bond (C=O)…

Q: What is the structure of the compound formed when 5-nitro-2-furaldehyde reacts with 4-cyanophenyl…

A: 5-nitro-2-furaldehyde is an aldehyde with -CHO group. 4-cyanophenyl hydrazine is a hydrazine with…

Q: What will the value of the molecular ion be for the product in the catalytic hydrogenation of…

A:

Q: Which of the following will test positive in the alcoholic silver nitrate test? 2-bromopropane…

A:

Q: In acid-base equilibria, the presence of an electron withdrawing substituent on the R- group of the…

A: The nature of alcohols (R-OH) is acidic. After the removal of proton (deprotonation), alcohol forms…

Q: 1 .CI Br 5 CI 3

A: Answer: Nucleophilic substitution is the characteristic reaction of alkyl halides where 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.