Show the arrow pushing mechanisms for the formation of the following. @ISoamyl acetate DOctyl Acetate

Q: Give the expected products for the aldol condensations of: a) Propanal b) 2-butanone

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Q: Show the two (neutral) organic starting materials that would be used to synthesize the compound…

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Q: d. ethanal + CH:MgBr followed by acid CH3- - H ethanoic anhydride + potassium butyrate е.

A: For the question d , Ethanol + CH3MgBr  CH3MgBr is a Grignard reagent , the reaction between Ethanol…

Q: Provide the reactants necessary to prepare the following compound using Robinson annulation.

A: The Robinson annulation is defined as a chemical reaction used for the creation of six membered ring…

Q: NABH4 МеОн of (CH3CH2)2NH, mild acid NaBH3CN H3CSH

A: The product of the reaction is given as follows

Q: Perform a retrosynthetic analysis and suggest a synthesis of the target molecule (on the left) from…

A: The Retrosynthesis method is the method that determines the starting material by the fragmentation…

Q: Write a curved arrow mechanism for the acid-catalyzed formation of the imine below: HO, NH2 LOH

A: Since there is a lone pair on N and partial positive charge on C attached to double bond O in…

Q: 2, Circle the phenols that would produce chemiluminescence following the proce

A: Chemiluminescence is a phenomenon of light emission in a chemical reaction. Phenols are acidic in…

Q: Complete the synthesis of the target molecules below (on the left) from the starting material (on…

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Q: Ex. Write the mechanism for the acid-catalyzed formation of the corresponding ether from: a.…

A: a. 1-butanol is a primary alcohol. It cannot produce a stable carbocation. The steric crowding…

Q: Show the electron-flow mechanism of the synthetic schemes (Carbon Tetrachloride) of the picture…

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Q: Using curved fishhook arrows, propose a mechanism for the formation of cyclone tame ring of…

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Q: Show the order of reactivity of the below-given compounds towards decarboxylation:

A: Decarboxylation is a chemical reaction. In this carboxyl group get removed and it leads to releases…

Q: Give all the reactions that alcohol could give products according to Sn1 Mechanisms.

A: SN1 reactions proceeds through carbocation intermediate. The order of the reaction is one i.e.…

Q: Show the electron-flow mechanism of the synthetic schemes (Aniline) of the picture below. This…

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Q: please help with this question. thank you.  Provide a detailed, stepwise mechanism for the…

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Q: What types of compounds give haloform reactions? show on examples

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Q: TRUE or FALSE. When phenol undergoes an FC alkylation with methyl chloride and aluminum chloride,…

A: We have to predict whether given Statement is correct or not.

Q: Show the process of synthesizing 2-methylpentanoic acid from diethylpropanedioate.

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Q: Please provide the 2 enol tautomers of 3-hexanone

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Q: Show the arrow pushing mechanism for getting tropylium ion from the benzylic carbocation

A: In the given question we have to rearrange the benzylic carbocation to tropylium ion.

Q: Show the step by step synthesis of the following compound.

A: First add Cl on benzene via Electrophilic substitution recation  Then reaction with NaOH which gives…

Q: Chemistry Please show the mechanisms for: Epimerization at alpha carbons (acid or base) Halogenation…

A: Epimerization is a process in stereochemistry in which there is a change in the configuration of…

Q: Show Dehydration Using POCl3 + Pyridine—An E2 Mechanism ?

A: Dehydration of alcohols with the help of phosphorus oxychloride POCl3 and pyridine (a base of amine)…

Q: When alcohol A is heated with base as shown below, the expected epoxide does not form. Explain why…

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Q: d. (i) Discuss the mechanism of the reaction sequence shown in Scheme 1, include all curly arrows in…

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Q: Do a retrosynthetic analysis on the following compound, ending withavailable starting material.

A: Unconjugated dienes have the double bonds separated by two or more single bonds. They are usually…

Q: g ease of acid-catalyzed dehydration.

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Q: Show the product and arrow pushing mechanism for the following reaction. Make sure that label the…

A: The product of the given organic reaction is as follows.

Q: Show the complete and detailed reaction mechanism (oxidation reaction) of 3-bromobenzyl alcohol in…

A: 1 CeCl3  is catalyst  act as Lewis Acid attact on       oxygen lone pair.

Q: At pH = 12, the rate of hydrolysis of ester A is greater than the rate of hydrolysis of ester B. At…

A: Concept introduction: Catalyst: Substance which helps in increasing the rate of a particular…

Q: Provide a plausible arrow pushing mechanism for the reaction below. 1.1 eq. tBuOK 2. acidic workup

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Q: Embed an image of a handwritten mechanism for the reaction between ethyl vanillyl alcohol and…

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Q: Predict the product of the Robinson annulation reaction between the diketone and alpha,…

A: first base will abstract the acid hydrogen and form thermodynamic enolate which was then attack with…

Q: Show the steps in the acid-catalyzed formation of a cyclic acetal from ethylene glycol.

A: Carbonyl reacting with diol forms cyclic acetal.

Q: +/ Haf 1. Dry El₂0 at-60° 2. aqueous NH, Cl at 0°

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Q: AICI3

A: It is an example of Friedel craft acylation reaction, Here a new cyclic ketone formed as the major…

Q: NH2

A: Retrosynthetic analysis is an analysis technique try to solve the problem for the synthesis of…

Q: Show a mechanism for the sulfonation of t-butylbenzene

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Q: Show the reaction mechanism for the formation of 2-chlorow-methylpropane from 2-methlpropene in…

A: The given reaction will proceed through carbocation as intermediate.

Q: Ph Ph Ph Ph Ph Ph Ph Ph

A: The retro synthesis of the target compound is outlined as:

Q: of NH

A: When Carboxylic acid derivatives, (acyl Chloride, ester , anhydride and amide) hydrolysed in basic…

Q: Using the "Basic" toolbox on OscerSyn, propose a synthesis of the following compound using reactants…

A: The synthesis method for the given compound has been described below.

Q: For the following reaction, provide an arrow-pushing mechanism and the product. Ph₂P. KOtBu e Br

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Q: Show the complete mechanism for the following four. Write the complete stepwise mechanism for this…

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

Q: 3-) Show the mechanism by using curved arrows for the reaction between following lactone and…

A: Question a compound of lactone is a reaction of ethyl magnesium bromide and H3O+ can be mechanism is…

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.