Q3/ Starting with toluene, how would you synthesize three different nitrobenzoic acids? Q4/ Draw a tetrahedral representation of (R)-3-chloropent-1-ene.

Q: (a) 2-methyl-1-iodocyclopentane + NaOCH3- --->A (b) A + (1) Hg(OAc)2, H20/(2) NABH4 ----> B

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Q: Can you draw the structure for: 2-hydroxycyclooct-5-enone

A: We have to draw the structure for the compound : 2-hydroxycyclooct-5-enone

Q: (a) What product(s) are formed when the E isomer of C6H5CH = CHC6H5 is treated with Br2, followed by…

A: a.

Q: (c) OH (d) Br ? ? Eight or fewer carbons Acyclic compounds OH Br

A:

Q: Draw a stepwise mechanism that shows how all three alcohols areformed from the bicyclic alkene

A: Hydration of alkenes is one of the methods used for the formation of alcohol. The general steps…

Q: Q 4: Comparing, Phenol reacts readily than the benzene, so it is a A. nucleophiles B. electrophile…

A: Phenol reacts readily than benzene

Q: How to Form an Internal Alkyne by Two Sequential SN2 Reactions ?

A: The terminal alkynes are those alkynes in which the triple bond is present between the first and the…

Q: a. How many alkenes could you treat with H2, Pd/C to prepare methylcyclopentane? b. Which of the…

A: Alkenes are unsaturated hydrocarbon with C=C bonds in the parent chain of the compound. Due to this…

Q: Draw the product of attached thermal electrocyclic ring closure.

A: Electrocyclic ring closure is an intramolecular reaction that produces a cyclic product containing…

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

A: Zaitsev rule: During elimination greater substituted alkene is predominantly formed.

Q: Name the following alkene and draw the product of the reaction with KMnO4.

A: The hydrocarbons in which two of the carbon atoms are bonded to each other by a double bond are…

Q: В. Н.С C=C CH3 С. Н Н c=c CH,CH3 A. H;C CH3 H H H. H H

A: Higher is the stability of alkene, lower is the heat of hydrogenation. Heat of hydrogenation ∝…

Q: R. Which of the following alkene has highest value of heat of hydrogenation? (a) (b) (c) (d)

A: The given alkenes are as follows.

Q: h. How do you convert 1,4 -Dibromo-2-butyne to Cis-1,4 -Dibromo-2-butene? i. How do you convert 1,4…

A: Cis Trans Configuration :- Cis Trans isomerism is also called geometrical isomerism. In alkene when…

Q: Show how to convert cyclopentene into Iodocyclopentane  compound

A: Cyclopentene is a five membered ring containing one double bond. Like all the alkenes,it also has…

Q: Rank the following substituted anilines from most basic to least basic:

A: Amine is a functional group in which nitrogen atom is attached with two hydrogen and one aromatic…

Q: H30* ?

A: In the presence of acid alcohol gets protonated and then water is eliminated to produce carbocation.…

Q: Which of the following carbocations (A or B) is more stable? Explain your choice.

A: In the given two carbocations, the stability is decided by the electronegativity factor of O and…

Q: Rank the alkenes shown from least exothermic (1) to most exothermic (4) heat of hydrogenation. a. b.…

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Q: Cuando se añade H-Br a un alqueno terminal el producto sigue la regla de Markovnikov. O a. Cierto O…

A: Note: According to our guidelines we are supposed to answer only one question.  Kindly repost other…

Q: Q9. The following structure represent a hydroxylated product of head-to-tail dimer of two isoprene…

A: Since you've posted multiple independent questions, we're solving the first question for you. If you…

Q: Draw a stepwise, detailed mechanism for the dienone–phenol rearrangement, a reaction that forms…

A: Please find below the reaction mechanism.

Q: What vinylic halide couples with styrene (C6H5-CH=CH2) in order to synthesize each of the following…

A: Heck Reaction: Heck reaction is a coupling reaction in which vinyl halides or aryl halides couple…

Q: CH3-C-0-CH₂CH3 Determine the products of reduction for the compound above A) B) C) O: D)…

A: Reduction of ester gives alcohol. In presence of strong reducing agent.

Q: halogenation (elimination) in resence of a strong base to give 2-pentene as the only alkene product?…

A: In the Elimination reaction carbocation is formed which can be re-arrange to get stability. So we…

Q: CF3 KOET ELOH, A SO,CH3

A:

Q: Draw the organic product that forms when the following compound is treated with aqueous. + NaOH…

A: The given molecule is treated with NaOH(aq)

Q: The compound cyclohex-3-en-1-one can give 2 carbanions. Point out the most stable and the reason?

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Q: Consider the four trienes E–H. Rank compounds E–H in order of increasing heat of hydrogenation.

A: Hydrogenation It refers to the treatment of substances with molecular hydrogen adding pair of…

Q: show the synthetic scheme to achive a final product L R-C-0-0-4 !! OH он 4 DR. CO₂ H 2) H₂ot Ⓒ

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Q: Draw the organic product(s) of the following reaction. NANH2 , NH3() CEC

A: Non terminal alkynes reacts with NaNH2 in presence of liquid ammonia and undergoes reduction…

Q: Question 1 What synthetic goal is achieved by subjecting an alkene to an…

A:

Q: Pyridine NaNg i) LIAIH4 (S)-Octan-2-ol -SO,CI A Меон ii) H20

A: First step is Conversion of OH to good leaving group this step also known as protection of alcohol

Q: Provide a curved arrow mechanism for the following reaction. CH;CH>OH + enantiomer

A: This reaction follows SN1 mechanism, In SN1 mechanism firstly leaves group leaves and carbocation…

Q: Draw the following compound on your separate sheet. (1S,2S)-5-(2methylepoxy)cyclopent-2-enol

A: Given name, (1S,2S)- 5- (2 methylepoxy)cyclopent-2-enol

Q: a) CH3 b) CH3 – CH – CH- CH3 CH3 с) СНЗ — СН2 —- CH - СHЗ

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Q: How to figure out E and Z fornalkenes?

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Q: Answer all questions Q1. What are the various ways by which alkenes maybe synthesized. Q2. Give…

A: SOLUTIONS: Step 1: alkenes are generally prepared through β- elimination, in which 2 atoms on…

Q: Draw the organic product(s) formed upon the addition of HBr to (a) 2-methyl-2-pentene, (b)…

A: Hydrobromination of alkene gives alkyl bromide product. Regioisomers are a class of constitutional…

Q: Draw the major intermediate and product of the reaction between (2E)-4-methylhex-2-ene and Br, in…

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Q: Draw the organic product(s) of reaction of the alkyne above with H3O+ in the presence of HgSO4

A: The alkyne given is having 7 carbon longest chain (7 grey balls in longest chain) with alkyne bond…

Q: Show how this alkene can be synthesized by a Wittig reaction. CHCH3

A: The Wittig reaction is the formation of an alkene compound by the transformation from the reaction…

Q: 2. Draw the major product of the following E2 reaction. Show stereochemistry where appropriate.…

A:

Q: What other alkene is also formed along with Y in Sample Problem 9.3? What alkenes would form from X…

A:

Q: Draw the products (including stereoisomers) formed when (S)-2,4-dimethylhex-2-ene is treated with…

A: Anti Markonikov rule  Alkenes on reaction with HBr in the presence of peroxide forms an addition…

Q: 6. Draw the reagent that converts the alkene below to the epoxide (oxirane) c=CH2 CH2 H,CH,C°…

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Q: MENH2 SO3ME MеHN. NEC- CI NEC a. Draw a reasonable arrow-pushing mechanism for this transformation.…

A: There will be removal of HCl.

Q: Draw the enol or keto tautomer(s) of each compound.

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

Q: Show which position of the 6 aromatic carbon is (are) the most electron rich by drawing detailed…

A: Electronegative elements(O/N) when directly attached to phenyl rings act as electron donating group.…

Q: Draw the equilibrium chair confirmation of cis1-chloro-3-methylcyclohexane. Interpret the E2…

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