OCH3

Q: Rank the following compounds from most reactive to least reactive in an electrophilic aromatic…

A: Electrophilic aromatic substitution: In an organic reaction in which an electrophile replaced an…

Q: The reaction of a ketone with an alcohol in acidic conditions will result in:     an alkane     an…

A: When ketones react with alcohols in the acidic conditions they result in the formation of acetals.

Q: The major organic product of the reaction of benzaldehyde with hydrazine is. N=N-OH CH=N-NH2 CH=N-OH…

A: This question is related to organic reactions.

Q: Benzene undergoes electrophilic aromatic substitution reaction with alkyl halide in the presence of…

A: Benzene undergoes electrophilic aromatic substitution reactions with alkyl halide in the presence of…

Q: How could the following compounds be prepared using an alkene as one of the starting materials?

A: Hello. Since your question has multiple sub-parts, we will solve first three sub-parts for you. If…

Q: Which of the following species is attacked by benzene in the electrophilic nitration reaction?

A: Electrophile is an electron deficient species that is attacked by electron rich species like…

Q: Which is an alkylation product of benzene? NH2 NO2 CH3 A В D

A: Alkylation product of benzene can be obtained by using a well known reaction known as Friedel craft…

Q: Identify the three products formed when 2-bromo-2-methylpropane is dissolved in a mixture of 80%…

A:

Q: Br2 (g) FeBr3 CI CI Br2 H2NNH2 В C (h) A FeBr3 AICI3 OH (Give all products) NH2 HNO3 (i) H2SO4

A: #(g): Br2/FeBr3 add a -Br group to a benzene ring. The reactant has two groups attached which are:…

Q: Rank the following alcohols in order of increasing ease of acid-catalyzed dehydration. Provide the…

A:

Q: The reaction of ozone with 2-butene leads to -10 formation of aldehyde + ketone 0 aldehyde + alcohol…

A: Here we have to determine the correct products formed by the ozonolysis of 2-butene .

Q: Acetals are formed from the reaction of two alcohols with a carbonyl under acidic conditions. Acetal…

A: During the acetal formation by 1,2-ethanediol and two molecules of ethanol, the same types of bond…

Q: Draw the resonance structure of the following intermediates in the nitration of phenol: OH =

A: The Resonance  structure  are as follows.

Q: 2B The hydration reaction of an alkyne is not a logical preparation method for each of the following…

A: The hydration reaction of an alkyne produces an internal ketone, never an aldehyde. The basic…

Q: ive the major product of the following Grignard reaction: Br T + Mg Ether What is the major addition…

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

Q: What reactions and reagents can be used to make phenol from benzene if electrophilic aromatic…

A: Solution You can prepare phenols in massive quantities by the shift of the Na salt of benzol…

Q: Muscalure is the sex attractant of the common housefly. Flies are lured to traps filled with bait…

A: Muscalure can be synthesized from 1-bromopentane.

Q: Draw the overall reaction of 1-butanol with HBr and H2SO4 to form 1-bromobutane.

A: Alcohol reacts with the hydrogen bromide from alkyl bromide in the presence of a sulfuric acid…

Q: Identify the best reagents to complete the following reaction. OH

A:

Q: 5. What is the structure of an intermediate in the methyl shift rearrangement reaction shown in the…

A: Since you have asked multiple questions we will solve the first question for you if you want any…

Q: H2SO4, H2O Choose the enol(s) that can be formed from the following oxymercration reaction. OH ОН OH…

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

Q: .CH (i) sO3 H2SO4 H2SO4 (k) CH3 Na2Cr2O7 (1) H*, Heat `C(CH3)3

A:

Q: Which of the following sequences of reactions would convert toluene to 2-bromo-4-cyanotoluene?

A: Alkyl group is ortho/Para directing group Nitro group is electron with drawing group hence its is…

Q: Acid-catalyzed dehydration of 3-methyl-2-pentanol gives three alkenes: 3-methyl-1-pentene,…

A: Since we know that acid catalyzed dehydration mechanism have carbocation as intermediate  And as we…

Q: Zaitsev's rule can be used to predict the major alkene product in a dehydration reaction. What is…

A: Alcohol gives dehydration reactions when it reacts with a strong acid like H2SO4 or H3PO4 to form an…

Q: What alkene is needed to synthesize each 1,2-diol using [1] OsO4 followed by NaHSO3 in H2O; or [2]…

A: The organic reactions help in the conversion of one organic compound into other compounds with the…

Q: ОН H3C- H3C- + ОН НО ОН A) NABH4, ethanol B (1) BH3, (2) H3O* 03, Zn/H20 D KMNO4, H30*

A:

Q: cyclohexanone 0

A: Cyclohexanone is a cyclic ketone. NaBH4is a reducing agent used in chemical reaction.

Q: Many hunting dogs enjoy standing nose-to-nose with a skunk while barking furiously, oblivious to the…

A: Using the chemical reactions how the mixture helps to remove the skunk spray from the dog has to be…

Q: Which one of the following compounds give racemic mixture when treated with NaOH (aq)?…

A: If both the enantiomer are formed equally then we get racemic mixture

Q: Draw the structure of the starting material needed to make 2-methylhept-3-yne using sodium amide in…

A: Given reagents is sodium amide in liquid ammonia and 1-bromopropane. Sodium amide will deprotonate…

Q: Give the product(s) formed when the following species react together: CH3CH2OH and-NH2

A: A substance that can give H+ ion is called acid and a substance that accepts H+ ion is called base.

Q: Draw the skeletal structures of all the final organic products formed when phenol (C6H5OH) is…

A: Given is two step organic reaction.The starting compound of given reaction is phenol.

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.