7. Synthesize ONE of the following benzene derivatives starting from benzene. F CI

Q: 22. Which of the following reactants will add symmetrically to alkenes? O a. H20, H2SO4 Ob. H2, Pt…

A: A multiple choice question based on alkenes, which is to be accomplished.

Q: Draw the structure of the alkene needed to synthesize the product shown using the reagents provided.…

A: This is an example of dihydroxylation of alkene with osmium tetroxide (OsO4). There is…

Q: Pls help ASAP

A: a) 2-methyl butanoic acid:- •Here carbon chain is of 4 carbon because there is -but- used. •Oic acid…

Q: What is the major organic product obtained for the following reaction? گرام NC,,. NC,, NC... NC. mon…

A: Williamson ether synthesis involves the reaction between an alkoxide and alkyl halide.. The reaction…

Q: 1 Give an example (molecular structures) of each functional group. Use arbitrary alkyl groups (e.g.,…

A: a) CH3-Cl Chloromethane CH3-Br Bromomethane CH2CH2-I Iodoethane b) CH3CH2-OH Ethanol CH3CH(OH)CH3…

Q: 17. Give IUPAC names for the following alkenes. a. HX b. s

A: Since,Rule of IUPAC-1) Longest chain as parent chain.2) Numbering start from those side where more…

Q: QUESTION 18 Which of the following alkenes is the most stable? CH;CH, CH; CH,CH3 Ola. Ob. H;C Oc.…

A: Question 18 is solved.  Alkenes are those organic compounds which contain one or more double bonds.…

Q: What is the product of this reaction? Click on a letter A through D to answer. TSOH (cat) А. В. C.…

A: Ketone and Cyclic amine is given in the presence of TsOH . Product = ?

Q: Which of the following compounds does not contain alkynes in its chemical structure? а. CH, b. H,C -…

A: Alkyne

Q: The reaction of CH;CH=CH-CH=CH, with excess bromine gives chiefly 1,2-dibromo-3-pentene b. 22. a.…

A:

Q: 41. Draw the structure of a hydrocarbon that has six carbon atoms and a. three vinylic hydrogens and…

A: Vinylic hydrogen is bonded to the vinylic carbon. The hydrogen is directly attached to the sp2…

Q: Name each monosubstituted benzene. a. H;C-CH, b. F C. CH3 H;C-C-CH,

A: a) The name of the given mono-substituted benzene is, Ethyl benzene

Q: Which of the following best describes why only small aldehydes and ketones are soluble in water? A)…

A: Aldehydes and ketones are organic molecules with a carbonyl group, i.e. a double bond between carbon…

Q: 1. Provide the IUPAC name for each of the following compounds. a. b. zu 2. Provide the correct…

A: The given molecules are examples of either cyclic or acylic ethers with variable carbon atoms.

Q: Identify the alkyne. a. O b. O C. O d.

A:

Q: aldehydes ar H.

A: We can combine this in presence of base. Such reaction is known as aldol condensation reaction.

Q: 8. Which of the following molecules can tautomerize? он a. 6. с. . II Ш OH OH II d. С. IV all of…

A: Keto-enol tautomerism is a chemical behaviour of organic chemistry, involving a state of…

Q: Identify reagents that can be used to achieve the following transformation: OH O 1) NaOH, 2) RCO3H,…

A:

Q: Circle all isoprene units in each of the given terpenes:

A:

Q: 1. Draw the structure of 4-ethoxy-2,2-dimethyldecane.

A: Given,The name of the molecule is:4-ethoxy-2,2-dimethyldecane

Q: 3. Which carbon would the Br of HBr add to in the following unsymmetrical alkenes? 1 Problem Set #7…

A: HBr is added to the unsymmetrical alkene according to the Markovnikov’s rule. The Br- is added to on…

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.