CH3 OCH3 (the Eisomer) CH,=CH-COCH3 Methyl 2-propenoate (Methyl acrylate)

Q: Draw the products, including their configurations, obtained from the reaction of 1-ethylcyclohexene…

A: Since you are asked for multiple sub-parts, we are entitled to solve first three questions.

Q: Which reagent would be best to convert cyclohexanol into chlorocyclohexane? O HCI AICI3 C12 O SOCI2

A: Which one of the following is correct

Q: 2. What is the best name for the following molecule? a. (S)-4-methyl-3-oxo-7-octene b.…

A: While writing the IUPAC name first identify the parent name and the functional group.

Q: 2. Reaction of this alkene to the different reagents in the arrows HCl CH,I,, Zn(Cu), ether BH3,…

A: A. Addition of HCl to unsymmetrical alkene follows Markownikoff's rule. That's why Cl^- adds to more…

Q: D (C3H1204) H30* heat heat E

A: A scheme is given to us . In this scheme we have to identify unknowns

Q: Which reaction would yield cyclopentanol? (A) (B) -d 8 (C) (D) 1. LiAlH4 2. H+ 1. NaBH4 2. H+ 1.…

A:

Q: Which structure is the most likely product of the reaction below? CHCI3, KOH -CI CI -CI -CI

A: CHCl3 form carbene with KOH then addition of carbene to double bond occur. ->Carbene added from…

Q: Which alkene when hydrochlorinated (hydrohalogenation reaction) will give this alkyl halide as…

A:

Q: Prepare 1-nonen-3-ol from heptanal and acetyle a. CH3(CH2)5CH(OH)-CH=CH2

A: Given is synthesis reaction.

Q: What alkenes are formed from each alkyl halide by an E1 reaction? Use the Zaitsev rule to predict…

A: E1 reactions: These reactions proceed in two parts. Lose of leaving group. Removal of proton These…

Q: What is the major product of the reaction of 2-hexyne with excess bromine? A) 2-bromohexene B)…

A:

Q: How to draw the potential energy diagram for this reaction? C₃H₈O (l)  → C3H6 (g) + H2O (l)…

A: Potential energy diagram of a reaction is the energy profile diagram plotted between the energy on…

Q: A single alkyl bromide reactant theoretically yields either of the given products, depending on the…

A: The reaction of an alkyl halide with CH3OH proceeds with the SN1 reaction mechanism and the reaction…

Q: Which reagent is appropriate for the following reaction yclohexene converted to trans-cyclohexane…

A:

Q: Draw a structural formula for the product of each SN2 reaction. Where configuration of the starting…

A: SN2  reaction: It is a nucleophilic substitution reaction in which the rate determining step depends…

Q: Show the reagents and experimental conditions necessary to bring conversion in good yield.

A: Given conversion reaction is:

Q: Draw all possible constitutional isomers formed by dehydrohalogenation of each alkyl halide. Br CH3…

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: What is the major monobromination product formed by heating each alkane with Br2? b.…

A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: Which set of reagents would give a meso product when reacted with cyclohexene? ? A. CH;CO,H B. (1)…

A:

Q: Which is an unlikely product of the following hydrochlorination of an alkene? CH3 H-C-CH=CHCH3 + HCI…

A: Since you have asked multiple question, we will solve the first question for you. If you want any…

Q: show the reaction of 2-methyl-2-butene and 2-methyl-1-butene with Br2 in CH2Cl2

A:

Q: Determine the reagents required to convert (CH3)2C=CHCOCH3 to each product. 2 H,O 2 H,0 2I H,0 12)…

A: Applying concept of organic synthesis.

Q: ). Draw all monochlorination products expected from reaction of chlorine with 3,4- dimethylhexane.…

A: In mono-chlorination reaction, the C-H bond of reactant breaks and new C-Cl bond is formed via free…

Q: 2. What Alkene would be used to synthesize 3-bromohexane? + HBr CH3CH2CHCH2CH2CH3 Br

A: You can start with 3-hexene. Since the molecule is symmetrical through its double bond, it doesn't…

Q: The compound below undergo elimination reaction to produce 2 types of alkenes. Based on Zaitsev…

A: We have given the organic reaction and we have to find the major product of the reaction.

Q: Addition of HCI to the unsymmetrical alkene below could potentially give rise to two products. C2H5.…

A: Addition of HCl to the unsymmetrical alkene is an electrophilic addition and occurs through…

Q: Draw the structure of the major product of 2-bromo-4-methyl-3-hexyne + Li in NH3

A: Structure of 2-bromo-4-methyl-3-hexyne is as follows. Valency of carbon is four but here it is…

Q: Give two sets of reactants (each set including an alkyl halide and a nucleophile) that could be used…

A: Please find below the first set of reactants

Q: Addition of HCl to alkene X forms two alkyl halides Y and Z. Label Y and Z as a 1,2-addition product…

A: To find: 1,2 addition and 1,4 addition product of the given reaction

Q: Show the reagents and experimental conditions necessary to bring conversion in good yield.

A: A chemical reaction is symbolic representation of the conversion of substances to new substances. In…

Q: B. What substituted alkene would you use in the Heck reaction to make the following products? (a)…

A: The substituted alkenes for the Heck reaction are giving below

Q: 2. Please give the order of reactivity of alkenes CH3-C=ç-CH3 CH; CH3 CH3-C=CH-CH3 CH3-CH=CH-H CH3 B…

A: With the increase in the number of alkyl groups attached to the double bonded carbons, electron…

Q: Show the reagents and experimental conditions necessary to bring conversion in good yield.

A: The given reaction is, CH3CH=CHCH3→CH3CH=CHCH2COOH The reactant is But-2-ene and the product is…

Q: Draw the organic product(s) of the following reaction. CH3 1. OsO4 2. NaHSO3 CH2

A: Osmium tetroxide on reaction with alkene produces cyclic osmate ester which on hydrolysis using…

Q: Complete these nucleophilic substitution reactions. In each reaction, show all electron pairs on…

A: SOLUTION: Step 1: The reaction of n-butyl bromide with sodium methoxide gives methyl propyl ether as…

Q: Show the reagents and experimental conditions necessary to bring conversion in good yield.

A: The reagents and experimental condition has to be given for given convertion.

Q: What is the product of this reaction sequence? Br Otrans-5-methylhex-2-ene O trans-2-methylhex-3-ene…

A: Since, you have multiple question. So, I will solved first question for you.  You can see the…

Q: Draw the structure of the product of the reaction between the compound shown below and H,SO,…

A:

Q: B. Arrange the following alcohols in order of increasing rate of reaction with the Lucas reagent. OH…

A: Lucas reagent is the equimolar mixture of Zinc chloride, ZnCl2 and HCl mixture . In presence of…

Q: Draw the starting structure that would lead to this major product under these conditions. Select to…

A:

Q: Write the main products of the following reactions: CH3 | а) CHз - CH - Сн- СН- CH, + НBr peroxide…

A:

Q: Complete the following nucleophilic substitution reactions. In each reaction, show all electron…

A: Given:

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: Synthesize the product starting from benzene. CH3 CH₂ C1 Cl₂ [A] AIC13 FeCl3 KOC(CH3)3 [C] [G] A [D]…

A:

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

A: Oxidation of alkenes is done by using OsO4 , KmNO4 for the formation of syn-diol. Here the word syn…

Q: 1. Which will be the major product if 3,3-demethyl-2- butanol to react in 85% of H3P04? a.…

A: Alcohol gives dehydration reactions when they react with a strong acid like H2SO4 or H3PO4 to form…

Q: Reaction between CH3OCH3 and H2NCH; will give the following compound. (a) CH;OCH,CH;NH2 (b)…

A: The reactant species are dimethylether and methylamine. When the given reactant react together their…

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.