a. -NH2 and b. N. and

Q: Is carvacrol more acidic or less acidic than phenol? Explain your answer.

A: Higher will be the stability of anion ( after removal of proton ) higher will be acidity

Q: some components of clove oil eugenol eugenol acetate B-caryophyllene HO clove oil hexanes (50 mL)…

A: Clove oil is an essential oil produced from clove tree. These clove trees are generally found to…

Q: What is the correct reagent for the llow OH ?

A: A component or combination given to a system to initiate or test a chemical reaction is known as a…

Q: How do you find Ka for the Bromocresol green

A: A weak acid is one that does not dissociates completely into its conjugate base and H+.  pKa of the…

Q: why pyrazole is more basic than pyridine?

A: We have to tell why pyrazole is more basic than pyridine.

Q: Write out the steps needed to separate hydrocarbon A and carboxylic acid B by using an extraction…

A: The steps involved in the extraction sequence used to separate the given hydrocarbon A and…

Q: Outline an extraction procedure by which you would separate a mixture of the following three…

A: Step 1 : mixture of compounds is treated with 10% HCl, aniline will go into water layer. water layer…

Q: (1) Which has the most acidic proton? (2) Which is a product after dehydration of two acetic acids?…

A: The solution to the following questions are provided below with detailed explanation and reasoning.…

Q: d) .F

A: benzene undergoes electrophilic substitution reaction due to pi-electron cloud over the whole…

Q: butene is produced. When potassium hydroxide is the base, 2-methyl-1-butene accounts for 45% of the…

A: This is the concept of elimination reactions

Q: Develop a flow chart to show how you can separate the following two compounds using acid-base…

A:

Q: Explain which position in indole will be susceptible to SEAr reactions

A: Indole has C3 position that is susceptible to SEAr, aromatic electrophilic substitution reaction.

Q: Answer questions a-c about the Bronsted acid-base reaction below using the identifying letters A-D…

A:

Q: Classity the solvents following pootic, Apootic and Amphipotic: as (i) CHCl3 () CH2 Coo H (iv) Hz…

A: Protic solvents are those which are having one or more labile H+ ions. This H+ will only be labile…

Q: Name a reagent which Ahmed can use to distinguish between a chloride, bromide and iodide ion…

A: The identification of cation and identification of anion of an inorganic salt is known as salt…

Q: atom sources. You may use any inorganic reagent necessary to complete your synthesis. A. С. B.

A:

Q: We expect 2-methyl-2-hexanol to produce a turbid; yellow clear; green clear; yellow turbid; green…

A: Note- Dear student since the given question is a multiple question hence I solved first question…

Q: Is this compound sensitive to base or to acid? Explain

A:

Q: а. NH

A: Answer Option a. Naphthalene and 1,2,3,4-tetrahydroisoquinolene. HCl is used in each case to…

Q: Why does the characteristic smell of vanillin disappear in the base solution?

A: In basic solution phenolic group of vanilin deprotonates and become phenolate ion,

Q: Write out steps to show how each of the following pairs of compounds can be separated by an…

A: Aniline and toluene can be separated by extraction procedure by following steps- Treat the mixture…

Q: Why is sodium hydroxide used in the smallest molar amount Explain the process of the "seeding"…

A: Since the NaOH is a strong base and it completely dissociates in an aqueous solution and produces a…

Q: : Starting from Benzene as the only organic reagent you have and use any other inorganic reagents to…

A: First step for synthesizing this compound is Friedel-Craft Alkylation reaction of Benzene: 1.

Q: Recommend the reagents

A:

Q: . When you are performing an extraction with diethyl ether and any aqueous solution, the bottom…

A:

Q: NINHYDRIN TEST 1) What is the principle involved in the Ninhydrin test? What is its purpose? 2)…

A: 1) What is the principle involved in the Ninhydrin test? What is its purpose- answer - principle…

Q: Basicity of Amines Table 9.6 Observations on the basicity of each test sample. Sample Observations…

A:

Q: Identify the following structure if it will give a positive result to Fehling's Test

A: Fehling's test is used for identification of aldehyde and ketone fo not give Fehling's test.

Q: (i) Describe two methods you could use to synthesise your tert-BuLi. Include in your answer any…

A: Tert-BuLi is an organolithium compound. It has many useful application in reaction chemistry.

Q: Noke Lew has a different unknown salt containing one of the nine anions used in this lab. She tries…

A: The three classification reactions for the analysis of anions are: 1. Formation of insoluble barium…

Q: Write out the steps needed to separate hydrocarbon A and carboxylicacid B by using an extraction…

A: In Organic Chemistry, Separation of non polar and polar substances is done using acid base…

Q: Question attached

A: To separate two compounds carboxylic acid and ether using acid-base extraction.

Q: Ethanol, Phenol, picric acid Arrange them according to the increasing acidity. Explain why and…

A:

Q: Table 7.4 Tests for phenols Positive Test Indicator Type of Organic Reaction Involved Test (i.e.,…

A: Qualitative test for phenols:

Q: Based on the informaton presented below, answer the following questions. An ether solution contains…

A: Ether is a very weakly polar solution that makes nonpolar and weakly polar organic molecules soluble…

Q: Do a retrosynthetic analysis on the following compound, ending withavailable starting material.

A: A species with a larger size can easily accommodate negative charge. In other words, in a large size…

Q: Suppose you have just synthesized heptanoic acid from heptan-1-ol. The product iscontaminated by…

A: SOLUTION: Step 1: Let sodium dichromate, sulfuric acid, 1-heptanol and heptanol be impurities. The…

Q: If the base was changed from NaH to LDA, the major product changes (shown below). Think critically…

A:

Q: Do a retrosynthetic analysis on the following compound, ending with the given starting material:

A: A species with a larger size can easily accommodate negative charge. In other words, in a large size…

Q: Write out steps to show how each of the following pairs of compounds can be separated by an…

A:

Q: How should you dispose of lauric acid/ benzoic acid after the experiment is complete?  Why?

A: The lauric acid/ benzoic acid is used in the experiment to determine the freezing point and melting…

Q: How would this compound react in ninhydrin test?

A:

Q: Investigate what an acid-base extraction consists of and what functional groups in substances can…

A: In Acid-Base Extraction, we can extract the acidic functional groups (like Carboxylic acid) and…

Q: Define Separation of benzoic acid and cyclohexanol by an extractionprocedure ?

A: Solvent used : Ethyl acetate Wash used to dissolve benzoic acid : NaOH Add water to this mixture of…

Q: Why is acetic acid used as reagent? What would happen if you used HCl instead?

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.