What is the name of Reaction 1 and 2? Choices: A. FC Acylation, B. SN Alkylation, C. FC Alkylation, D. None of the choices What is the Reagents for Reaction 1? Choices: A. CH3MgBr in ether, B. HCl, C. CH3NH2, D. none of the choices What is the Reagents for Reaction 2? Choices: A. ethanoyl chloride/AlCl3, B. ethyl bromide/AlBr3, C. bromoethane/FeBr3, D. none of the choices

Q: Which product below would be most likely to form after treating 1-propanol with TsCI, py followed by…

A: At first propanol react with TsCl,py form -OTS  , which is good leaving group, then in LiAlH4…

Q: 2. Rank the following, with 1 being highest, or most. (2 points each) OH HO Ability to decarboxylate…

A: Step 1: Beta keto carboxylic acid s are easily decarboxylate under thermal conditions Aldehyde s are…

Q: Reaction of the iodide I with KOH can result in two elimination products, the alkene II and the…

A: This reaction will prefer to go with E2 mechanism because KOH is strong base and in E2 mechanism we…

Q: Will you double check the attached images of reactions with my answers... (My answers are shown in…

A: In most of the reaction nucleophile substitution is taking place. Also, HVZ reaction, bromination…

Q: 1. NASH 2. H₂O

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

Q: Which of the following statements is INCORRECT? Select one: O a. Ethoxide is a better nucleophile…

A:

Q: 1) TSCI 2) NaOEt PQ-13. What is the major product of this reaction? Me H (В) Me OEt (A) OEt Me (D)…

A: We are given the reagents Tscl and NaOEt. It is a basic reagent.

Q: a. d. e. Predict the major organic product(s) of each reaction below. For reagents over the arrow,…

A: HydrogenationHalohydrin formationHydroboration oxidationOxymercuration-demercurationWilliumson ether…

Q: Write reactions of But-1-yne with the following reagents: a. Br2; b. HOH/Hg2+/H+; c. H2/Ni. d.…

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Q: From the lists of available reagents select the one(s) you would use to in a preparation of…

A: Step 1:  Step 2:  Step 3:

Q: a. b. C. 1 CI 2 досна 3 Draw a mechanism for the basic hydrolysis of these derivatives. 4 NHCH3 Rank…

A: Here, OH- will attack at the electrophilic C centre of C=O, and the leaving group will be released.…

Q: Select the reagents for the following transformation. Please enter your answer as a string of…

A: Detail mechanistic pathway is given below to find out the necessary reagents to accomplish the…

Q: 1.) LDA 2.) H. 3.) H3O* of

A: LDA acts as base abstract acidic hydrogen's  and produce carbanion  LDA useful in C-C bond formation

Q: 0. Rank the following molecules in order of decrea H I CF3 O F- II CF3 FO H3C III CH3 FO

A: This is general question from general organic chemistry.more the partial positive developed at…

Q: 2. Purpose a mechanism for the following reactions: а. Нeat +NBS Peroxide b. Heat +NBS Peroxide

A: We have to propose a mechanism for the following given reactions in step 2 as follows:

Q: d. f. + Cl₂ 0 °C HI 85 °C 40 °C

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Q: Predict the major product and provide a mechanism for the following: a.…

A: Organic reaction mechanism is the method of analysis in which we actually know how the actual…

Q: QUESTION 19 Select the most like products that would be produced from this serles of reactions. ONa…

A: Claisen Reaction This reaction occurs between two ester or one ester and one alkyl halide to give a…

Q: 1. Provide the major organic product for each of the following reactions. a. b. d. e. f. OH it OH OH…

A: Epoxidation of alkene takes place on reaction with peracids.CrO3, H2SO4 oxidises primary alcohol to…

Q: None

A: Step 1:  a. Identify the electrophile and the nucleophile:Electrophile: The carbon attached to the…

Q: Which of the following compounds will undergo aromatic nitration most rapidly? I NO2 II CI III IV…

A: A. IExplanation:The compound that will undergo aromatic nitration most rapidly is I. This is because…

Q: What is the organic product formed by the following sequence of reactions? Select one: O A. II OB.…

A: Option B is correct.Explanation:

Q: 1. i) Fill in the boxes with the missing reagent(s). ii) Label each reaction as an "oxidation" or…

A: As per your request for the solution of 1(a) and 1(d) . I'll solve these two questions.

Q: What is the most proper name of the following epoxide? a. (2S)-2-(2,2-dimethylbutyl)oxirane b.…

A:

Q: What is the product of the E2 reaction of (R) 3-bromo-2-methylhexane with OH Select one: O a. (Z)…

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: For the following reaction: a. Propose a mechanism b. Explain why 2 products are formed c. Explain…

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Q: The reaction mechanism for Reaction 1 is _____ Choices: A. SN1, B. SN2, C. SN Acyl, D. None of the…

A: In the above given reaction scheme, alkyl halide is first converted to thiol and then it is further…

Q: The quality of the substituent for the elimination reaction is the leaving group ability of it. Like…

A: The best leaving group has to be identified.

Q: From the lists of available reagents select the one(s) you would use to in a preparation of…

A: The question is based on the concept of organic synthesis.  we need to synthesize the product using…

Q: HCIO is a weak acid (Ka = 4.0 × 10-8) and so the salt NaClO acts as a weak base. What is the pH of a…

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Q: Which of the following halide can give best SN2 REACTION?

A: In the SN2 mechanism, nucleophile(Nu-) attacks the carbon atom to which the leaving group is…

Q: An SN2 mechanism takes place when 3-(bromomethyl)pentane is added to each nucleophile listed below.…

A: Concepts of SN2 reaction.

Q: a. Which of the following compounds cannot be prepared by a Heck reaction?b. For those compounds…

A: Introduction: Heck reaction: Heck reaction is used to synthesize the substituted alkene. It consist…

Q: apologies. There was an error for the names. Reaction 1 and 2 are different.  Possible answers for…

A: The answer is as follows:

Q: 9. Select reagents from the table to show how you would carry out these transformations. You should…

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Q: 16. Give the major product of mononitration of the compound. 17. -OCH3 Give the product of the…

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Q: The Hofmann product is favored by the E2 mechanism when 2-bromo-3-methylbutane is added: A. MeOH B.…

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Q: a. Provide the structural formula of each product for the reaction shown below: Et N H₂C OH b.…

A: A chemical reaction in which an electron-rich moiety attacks the electron-deficient atom and…

Q: The quality of the substituent for the elimination reaction is the leaving group ability of it. Like…

A: In elimination reaction atom/ group of atoms that leave the substrate is called leaving group. Speed…

Q: What is an appropriate stepwise synthesis for the following synthesis that uses ethyl…

A: Find out suitable reagent for conversion of reaction.

Q: Choose the product which derived with high yield in the following reaction: CH3-CH=CH2 + HBr ->…

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Q: the epoxide shown will react in acidic methanol to generate which product. Select one: a. None of…

A: Given is organic reaction.The given starting compound is epoxide.This is epoxide ring opening…

Q: 17. What reagent(s) would be required to accomplish the transformation shown? C=CICH₂ a. H₂, Pt c.…

A: Alkynes can be selectively reduced to an alkene by reaction with hydrogen in the presence of…

Q: .i) Circle which of the following is the most efficient synthesis of 1-butene:

A: Given : structure of reactants

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.