1.) 2.) Br

Q: This ether can be made using a Williamson ether synthesis. The possible bond disconnections are…

A: To find: The Williamson ether synthesis which will produce the higher yield.

Q: Show the stepwise mechanism for the reaction between methanoyl bromide and  methyl amine.  Use…

A:

Q: 3. (2) Outline an efficient synthesis of butyl iso-propyl ether, Start with alcohols of four carbons…

A: To synthesis molecule Butyl isopropyl with help of nucleophilic substitution reaction (SN1)…

Q: By means of a series of equations outline a method for carrying out the ff. conversions. You may use…

A:

Q: ОН and

A: Alcohol will not give 2,4 DNP test whereas alcohol after converting to alkene will decolourise…

Q: Q1. Outline two methods of phenols synthesis. Q2. Give a concise account on the nomenclature of…

A:

Q: What reagents are necessary to carry out the conversion shown?

A: Given that : We have to identify the reagents used for the following conversion :

Q: Offer an explanation for the observation that 4-chloropyridine is more reactive toward nucleophiles…

A: The reason why 4-chloropyridine is more reactive towards nucleophiles when compared to…

Q: Explain why methyl propyl ether forms both methyl iodide and propyl iodide when it is heated with…

A: Methyl propyl ether forms both methyl iodide and propyl iodide when it is heated with excess HI has…

Q: c) Illustrate a step-wise mechanism for the formation of compound X that comes from compound A.

A:

Q: Write a mechanism for the following reaction

A: The details solution for this is provided below in attach image.

Q: If a large excess of the nitrating reagent is added, does the product produced contain one nitro…

A: Given: Excess of Nitrating mixture To find: Product will have one nitro group or more than one nitro…

Q: Give the stepwise mechinism. Provide each step in this mechanism. Include curved arrows to show the…

A:

Q: 2. In a Williamson Ether Synthesis of Phenacetin When the reaction is complete, water will be added…

A: In the synthesis of phenacetine sodium acetamido phenolate reacts with ethyl bromide to form the…

Q: Which solvent would be used for a reaction using a Grignard reagent (RMgX)?

A: The solvent with no acidic hydrogen is used in case of grignard reagent reaction.

Q: Give a clear handwritten answer with explanation....complete the following reactions with missing…

A: In this question, we will identify the reagents and also give explanation.  You can see below all…

Q: Draw structural formulas for the α,β-unsaturated aldehyde or ketone and the lithium diorganocuprate…

A: The reaction of a α, β-unsaturated aldehyde and Gilman reagent is a vital tool in organic synthesis.

Q: what is the abstarct of the williamson ether synthesis experiment

A: Williamson's ether synthesis: It is used to prepare both symmetrical and unsymmetrical ether. It…

Q: In both SN1 and SN2 tests, why should 2-chlorobutane react more slowly than 2-bromobutane?

A: We are authorised to solve only one question at a time. Please post rest of the questions…

Q: 3. Upon treatment with aqueous acid, compound 1 is converted into compound 2.

A:

Q: f 1-phenylazo-2-naphthol (or Sudan I), phenyldiazonium reacts with β-naphthol. Draw the resonance…

A:

Q: Are the following statements are True or False   a. In addition to 1,3-dicarbonyl compounds, 1,4…

A: Pyrazole  Derivative are the 5 membered  ring having adjacent  Nitrogen Group

Q: Usually the keto form of a molecule is more stable than the enol form, for the following three…

A: keto form of compound which are showing tautomerize to form enol

Q: Which solvent should you use if the three compounds below are dissolved in ether and you want to…

A: Introduction: Extraction is the process of the separation of a substance from a matrix. The most…

Q: Explain why the acid-catalyzed dehydration of an alcohol is a reversible reaction, whereas the…

A: Generally, electrophile attack is the first step in the electrophilic addition of alcohol. The acid…

Q: Complete the arrow pushing mechanism from the benzyl chloride to the benzyl alcohol by adding…

A:

Q: 2. Write a synthesis of the Wittig reagent C1

A:

Q: 1) Outline reasonable synthetic schemes to convert pentane to 1-tritio-1-butyne 2) Draw a reasonable…

A: Given:-

Q: Below are several common solvents in organic chemistry. Select those that would not be compatible…

A: Given : structure of molecules Grignard does not react with ether, alakne, benzene

Q: Explain why the C=C of an enol is more nucleophilic than the C=C of an alkene, despite the fact that…

A: The electron pair availability or nucleophilicity depend upon the two factors: 1. Resonance 2.…

Q: A Wittig reaction occurs when 4-methylbenzaldehyde and benzyltriphenylphosphonium chloride are…

A: wittig reaction  used to  preparation of  alkene from a reaction between  carbonyl  (aldehyde or…

Q: Draw geometrically clear picture of the most stable enol form of the compound shown below, and point…

A:

Q: In what major form would this diol-aldehyde exist? Н НО ОН НО. НО -ОН НО. B НО Он НО, "ОН D

A: The major form of given diol-aldehyde exist can be drawn as

Q: Consider the tetracyclic compound with rings labeled A–D. (a) Which ring is the most reactive in…

A: Benzene ring is activated towards electrophilic substitution reaction if there is an electron…

Q: Which pair(s) can be separated by chemically active extraction? |-CH3CH2NH2 and C,H5NH2…

A: The pairs of organic compounds given are I. CH3CH2NH2 and C6H5NH2 II. (CH3CH2)3N and CH3CH2NH2  III.…

Q: Explain why compound A will not undergo a ring-opening reaction under thermal conditions, but…

A: Ring opening reactions for A and B are given below :

Q: 1) Which one more reactive to word nucleophilic substitution P- nitro toluene or O- ethyl toluene ?…

A: P-nitro toulene will be more reactive towards nucleophilic substitution than O-ethyl toulene because…

Q: Explain why compound A will not undergo a ring-opening reaction under thermal conditions, but…

A:

Q: Explain why compound A is much more stable than compound B.?

A: The compound A is more stable than compound B has to be explained below,

Q: 2. Reactivity of Aldehydes and Ketones a. Rank the following aldehydes and ketones in order from…

A: Given: Aldehydes and ketones : A, B, C, & D. The increasing order of reactivity is as follows:

Q: 1) Outline reasonable synthetic schemes to convert pentane to 1-tritio-1-butyne 2) Draw a reasonable…

A: Here we have to synthesize 1-tritio-1-butyne from pentane by multistep reactions.

Q: a. Which compound would you expect to have a greater dipole moment, methyl acetate or butanone?b.…

A: The solutions for both the subparts are given in the following steps.

Q: 1. Compound2 may have an electrophilicreaction because of its saturation 2. Compound1 must undergo…

A: Since double bonded and triple bonded compounds are in unsaturation condition whereas single-bonded…

Q: Br

A: In this question, we have to find out the correct answer of given problem by the help of Wittig…

Q: Regarding an organic chemistry laboratory experiment: a. In this experiment, the distillate is…

A: 1 ) Diethyl ether is highly volatile , flammable so keep away it from heat sources othrwise…

Q: 1. Explain the solubility behavior of the alcohols and phenols in water as a function of: a.…

A: (1) It is observed that Alcohols are more soluble in water due to formation of Hydrogen bonding…

Q: Is UV spectroscopy a correct method to distinguish between the Rectant and Product

A: UV Spectroscopy Absorption spectroscopy or reflectance spectroscopy in the ultraviolet-visible…