Give the structure of the major organic reactant(s) that combined to give the best yvic for the condensation (by water loss) products.

Q: alky benzene, group compound A, C§H$O, an optically inactive compound. They discovered tha compound…

A: Aromatic hydrocarbons are compounds with a benzene ring and substituted groups of elements. There…

Q: Write the complete reaction and give the IUPAC name of all structures (reactants and products) from…

A: The first step is the formation of the Grignard reaction, which reacts with carbonyl compounds to…

Q: Write down the reduction reaction of each molecule using appropriate reagents, listing the following…

A: The reduction of the given compounds are shown below: 1. The reaction of aldehyde in the presence of…

Q: 3. Illustrate all the possible reaction for toluene.

A: Toluene contain methyl group in benzene ring and it is electrons donating group because CH3 donate…

Q: Which of the following is a correct practice in handling reagents?

A: Option D. Clean up any spills after finishing the laboratory work.

Q: CI СООН CH3 NO2 A B C D

A: The electrophilic substitution reaction depends on the Group present in the ring .

Q: COMPLETE THE TWO REACTIONS BELOW

A: Fehling's reagent is reduced by only that aldehyde which has no alpha hydrogen and aldehyde is…

Q: An unknown hydrocarbon G, whose formula is C16H26 contains two triple bonds. Ozonolysis followed by…

A: Ozonolysis: Ozonolysis is an organic reaction where the unsaturated bonds of alkenes, alkynes,…

Q: What does alkyl halides gives on heating with dry Ag2O ?

A:

Q: Like alcohols, ethers undergo a cleavage by breaking a carbon–carbon bond between an alkyl group and…

A:

Q: (a) Illustrate the following name reactions by giving example :(i) Cannizzaro’s reaction(ii)…

A:

Q: A compound having the molecular formula C22H32O2 was isolated in 66% yield in the following…

A: Olefin metathesis 1-In olefin metathesis, two olefin compounds form a four-membered ring…

Q: 1. HNO3, H,SO, 2. Fe, HCI 3. NANO,, HCI 4. HBF, 5. KMN04, A CH(CHS2

A:

Q: Starting with acetylene and ethylene oxide as the only sources of carbon atoms, show how to prepare…

A: Q) Preparation of Hexanediol:

Q: showed the synthesis of dec-3-yne by adding the hexyl groupfirst, then the ethyl group. Show the…

A: The formation of but-1-yne from acetylene is as follows,

Q: HO

A:

Q: Outline the synthesis of the following compound using only acetylene and/or simple alcohols.…

A:

Q: HBr, CH;00CH3, hy CgH,,N CH;I C3H2,N

A:

Q: Treatment of propylbenzene with NBS + hv affords a single constitutional isomer. Suggest a structure…

A: The product formed is as follows:

Q: 2H2 CH,CH,CH,C=CCH3 Lindlar Pd Give the structure of the ommited in the reaction|

A:

Q: Provide the structure of the main product.

A: In this question we have to tell the main product of the reaction.

Q: Write a synthetic scheme (senes of reacthions) mduding the sleps and reagents to prepare the…

A: In the reactions given above benzene is the starting material.

Q: Give the major organic product(s) for the following reaction. Write NR if a reaction does not…

A:

Q: Aniline is oxidized and then resulting product is boiled with Conc. HNO3 and conc. H2SO4c

A:

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

A: Given ; reactant

Q: Draw the structure(s) of the organic product(s) predicted when this compound reacts with NABH4,…

A: NaBH4 acts as a reducing agent in organic reactions. In presence of carbonyl groups, the BH4-…

Q: II. Explain through the use of general reactions and brief statements the following phenomena: a How…

A: The carbonyl compounds (aldehydes or ketones) on treatment with LiAlH4 or catalytic reduction…

Q: BuLi -Br Ph3P A В + ↑

A: This reaction is Wittig reaction. Alkene is produced from carbonyl group.

Q: Complete the reactions below.

A: a)  Cyclohexanone is a Ketone.  In ketones carbonyl carbon is electron deficient, hence ketones…

Q: 1. what are the differences between acyclic and cyclic forms in terms of their physical properties?

A: Note - Since you have asked multiple questions, we are bound to solve only the first question for…

Q: HO ОН `ОН H₂CRO4 H2O PCC DCM MnO₂ acetone

A: -> H2CrO4/H2O is reagent used for oxidation of every alcohol. -> PCC/DCM is reagent used for…

Q: Illustrate all the possible reaction for toluene.

A: Toluene shows good reactivity for electrophilic substitution reactions. It is basically an aromatic…

Q: Give the structure of the major product (s) for the reaction listed below:

A:

Q: base C14H220 + H2O CH3

A: Given reaction is :  Give a structure of product given below= ?

Q: HO

A: - Provide all of the steps and reagents required for the following chemical conversion. More than…

Q: Compounds containing deuterium (D = 2H) are useful for kinetic studies and metabolic studies with…

A: Deuterium exchange takes place when acidic hydrogen is present. LiAlH4 reduces aldehyde into…

Q: Quinolines, heterocyclic compounds that contain a pyridine ring fused to a benzene ring, are…

A: When para-ethylaniline is used instead of aniline.

Q: Provide the reactions needed to product the products from the given starting material

A:

Q: In which of the statements given below, the event is not an oxidation reaction? A. Reaction of an…

A: The reactions in which the oxygen content of product increases or the hydrogen content decreases,…

Q: A compound with the molecular formula, C,,H0 was treated with Wolff-Kishner reagent and the product,…

A:

Q: Give Reaction of +NO with 1° Amines ?

A: Given reaction,

Q: Synthesis of Fenclorac starting with benzene? Show all reagents and all intermediate structures.…

A: The given compound is fenclorac.

Q: он он но, PRODUCT но А. В. С. D.

A: NaBH4 is a reducing agent. It can readily reduce aldehyde and ketone. But ester group can’t be…

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.