1. Propose a synthesis for the following example. H CO₂Me OH

Q: Provide the starting material for the following reaction. 1. MCPBA 2. H-O, -OH + en DH

A: alkene on Treatment with m-chloroperoxybenzoic acid leads to epoxidation which on reaction of…

Q: 1. What would be the best base for performing the elimination reaction shown? 2. What major…

A: Given : structure of reactants  Tip : strong base prefer E2 reaction.

Q: Choose the reaction conditions to complete the acid-base reaction shown. NaH CH3CH2OH H C:O A B C D…

A: Hex-1-yne is given, hydrogen on triple bond will act as strong acid, we can use strong base to make…

Q: None

A: Here is the visual representation of the reaction mechanism for the acid-catalyzed substitution of…

Q: what is the product?

A: Given is organic reaction.The given starting compound has two functional…

Q: Using Curved Arrows in an Equation Use curved arrows to show the movement of electron pairs in each…

A:

Q: NH,NH, Base

A: The above given reaction is Wolff Kishner reduction in which ketones and aldehydes are converted…

Q: 1. Rank each set of three alcohols in terms of increasing acidity, "1" being least acidic, and "3"…

A: - Inductive effect increases the acidic strength of the compound.  More is the number of…

Q: ) Rank the following in order of increasing boiling point. он но, CH3 A B C Depk the follewin g in e…

A: Boiling point is defined as the amount of heat required to vaporize a liquid.   this depends on…

Q: Question 4 Predict product: HO Question 5 Predict product: -OH COOH H,CO,C. H+ remove H₂O B COOCH…

A: Esters can be converted into Carboxylic acid and alcohol under both acidic and basic…

Q: 6. Rank the following compounds in order of most basic to least basic. ex M 11 III IV

A:

Q: hich of the following compounds has an acidic group? A NH₂ года о ная тень D NH₂ B E НО ОН "H ОН о я…

A:

Q: sider the following unequal equ in this equilibrium represent t er base? CH3 + CH3NH 2 ?

A: Acid is substance which release hydrogen ions and bases is substance which released hydroxyl ions…

Q: What is the major product of the following reaction? ملال له من H excess C. OH Ph HO ethanol OH Ph…

A: Aldol reaction organic reaction in which enolate ion reacts with a carbonyl compound to form…

Q: Choose the most acidic compound from Compounds l-IV. H. O,N-CH,-C-CH; OFt II III IV

A: The given compounds are : We have to determine which compound is the most acidic.

Q: Which is a stronger acid?

A: Acids are the compounds that donate a proton and becomes a conjugate base. a. CH3OCH2CH2OH is more…

Q: b) Rank the following alcohols from the most to the least acidic. НО. . CI . Н H3C-C-CH3 Н НО. " OH…

A: To find the order of the most acidic to least acidic alcohols, we will look at the conjugate base.…

Q: Which is the strongest acid? В. CI 0 FO | CH;CHCH,COH CH;CH,CHCOH CH;CH¿CHČOH CHCHC-COH F CI

A: We are having four organic compound that are acidic in nature, we have to predict the most acidic…

Q: Draw carborgl. a mechanism to convert an organo borane to a

A: Organoboron compounds are compounds of C and B. An organoboron is an organic derivative of boron.…

Q: Rank the hydrogen on the following compound in order of increasing basicity. (only mark the numbered…

A: We have to give the increasing basicity order of the given compound. Concept: Greater the s-…

Q: 11. Identify compounds A and B in the scheme below. OMs DBU (bulky base) Boc Compound A? HBr…

A: Bimolecular elimination reaction (E2) which occur in one step. In E2 reaction C-H bonds and C-X…

Q: 4. Put the compounds below in order of their basicity. Li в E > most basic least basic

A: Bronsted-Lowry acid-base theory: According to the Bronsted-Lowry acid-base theory, acid is a…

Q: Give the structure of the principal organic products.

A: Hello. Since the question contains more than three sub-parts, the first three sub-parts shall be…

Q: - - " 3. Rank the following carboxylic acids in the order of increasing acidity in an aqueous…

A: The objective of the question is to rank the given carboxylic acids in the order of increasing…

Q: CH,COOH NaOH

A: -OH is not a good leaving group ,it take H+ from acid and converted to good leaving group H2O+ ,so…

Q: Br trace .CH.CH,CH; acid HCI, H2O Y ZI +

A: In this question we have to tell the product of the reaction and the reagent used.

Q: Give the molecular formula corresponding to this structural formula. You may wish to review Sect.…

A:

Q: 3) In which set are the compounds arranged in order of decreasing acidity? A. 2-bromopropanoic…

A:

Q: A 20 ml sample of water from the Taal lake was brought to the laboratory for analysis. The dissolved…

A:

Q: In the Micheal addition below, which carbon is most likely to lose a proton to the base? H3C A A B C…

A:

Q: Select the major product of the following reaction. + 10% NaOH 50 °C ОН HO, ph ph ph ph II III IV O…

A:

Q: Provide the IUPAC name for the following carboxylic acids. What is the common name for the…

A: a) The longest possible carbon chain in the molecule is of 2 carbon as shown below with carboxylic…

Q: Of the following carbonyl compounds, which will contain the lowest percentage of hydrate when mixed…

A: Greater is the reactivity of the carbonyl higher will be the percentage of hydrate.  In case of…

Q: Carboxylic Acid Resolve the reactions.

A:

Q: Which of the following is the strongest base? A. (CH3)3COH B. CH3CH₂NH™ C. H₂O D. CH3NH2

A: We have given 4 molecules and we have to find  the strongest base among them.

Q: Draw the most likely conjugate base resulting from this acid-base reaction. Include all lone pairs.…

A: Step 1: When a proton is removed from hexanenitrile, it becomes its conjugate base (also known as…

Q: h. xs acetic acid + sodium hydroxide in water A CH3- - OH Na O4 Please Do these 2 Question the Way…

A:

Q: NAOH H_O 1) NANO, HCI Sn HCI O:N- -OH + C (C,„H,,0,N,) Br В OH 2) Fenol

A: Conversion of one organic molecule to another molecule is one of the important synthetic root in…

Q: Rank the derivatives of phenol in order of increasing acidity (Please explain) 

A: The compounds given are,

Q: 1. NaOH 2. NaOH, A 3. EtMgBr 4. H3O* :OH H :0: :OH 1

A:

Q: eaction #12 Figure #12 OH H₂N compound A + NH₂ OH compound B HN compound C OH N OH compound D

A: There is no any condition is given so this will simply go as acid base reaction.

Q: None

A: The question is asking for the product of the reaction between hydroxide ion (OH-) and hydrobromic…

Q: a. b. ·N· CH 3 Br. 1. PhMg Br 2. diluted H+ -O excews СПЗ Сигон Catalyst ficl

A: Given are reactions of ketones. First reaction is addition of Grignard reagent.  Second reaction is…

Q: How can th following synthesis be accomplished? OH

A: In given reaction,  alcohol is converted into alkane. Here, alcohol has 6 carbons but alkane had 9…

Q: Don't use hand raiting please

A: Lithium diisopropyl Amide (LDA) is lithium containing base. It is bulkier base used for the…

Q: acidity a

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.