Na;CO, 0N H2 CH,-C-I 0N. NaI DMF NO NO2 3,5-Dinitrobenzoic Acid lodoethane Ethyl-3,5-dinitrobenzoate

Q: 9. Draw the structure of product, substrate or condition in the following reactions (should clearly…

A: Reaction a , b , c -

Q: a) Complete the mechanism of the initial step of the reaction of the alkyl halide with sodium azide…

A: Reaction mechanism of chlorocyclopentane with sodium azide is drawn as,

Q: Explain the mechanism of the following reactions and give the name of product? CH,CH(OH)C(CH,),…

A: (a) dehydration of alcohol  (b) Addition of H2O to alkene in presence of H+

Q: Q/ Show the structures of the carbocation intermediates you would expect in the following reactions…

A: Please find the attachment

Q: Draw the structures for the intermediates and product (left to right) as represented by A to C in…

A: In this question we have to tell the product of the reaction sequence.

Q: NH2 NH. HO-P-O Br, in H,O OH ОН ОН Вa(ОН). е.

A:

Q: LOME O3 then Me,s Me 1) Вн, 2) H,Oz/NAOH/H,0 H. Me он -D Me Me (2) Hint: D (deuterium) is a stable…

A:

Q: Which of the following is the product of the acid-catalyzed reaction between acetone (CH3COCH3), and…

A: The mechanism for the acid catalysed nucleophilic attack of methylamine on electrophilic carbon…

Q: R-O-p-0. R mhm Oxidation mCPBA RO OR O-P-O to mhmm

A: mCPBA is oxidising agent.

Q: 4. Show the mechanism for the interconversion of the compounds below. Hint: They go through a…

A: In the presence of base acetone make enolate. Enolate acts as anucleophile and undergoes Michael…

Q: CH3 1) MCPBA 2) CH3NH2

A:

Q: 23. Rank the following substrates in increasing order of rate with CH3CH2S:, under SN2 conditions.…

A: SN2 mechanism proceeds via a single step reaction in which the nucleophile attacks on the reactant…

Q: MeO MeO. OH 5.0 eq. Li, ETOH HO. liq. NH3 MeO OMe OMe

A: In presence of Li/ liq NH3 or Na/ liq NH3 benzene undergoes birch reduction. Due to birch reduction…

Q: (c) What would be the product of the following reaction? Draw the reaction mechanism, propose a…

A:

Q: 7 Draw the structure of the product, substrate or condition in the following reactions (should…

A:

Q: 3. The reaction of (R)-2-bromopentane with NaOH in ethanol produced a racemic mixture. Br NaOH…

A: The details solution for this reaction is provided below in attach image.

Q: Me HI d) F3C H OH Br Br2 f) Br

A: In the first given reaction, halogen-substituted alkene reacts with hydrogen halide to give a…

Q: Draw the products of the following ozonolysis reactions: 03 (1) Me₂S 03 (2) Zn, HCI ?+ ? ?+ ?

A: In this question we have to tell the product of the reaction.

Q: (a) OTs NaH OH (c) PPH3 R HO, R 12

A: ->NaH is base which can abstract acidic hydrogen. ->PPh3 / I2 give substitution reaction.

Q: 1. Determine whether the following reactions will proceed via an Sn1 or Sn2 mechanism: CI NaOH DMSO…

A:

Q: In CHM 235, you will learn that the Michael reaction of ethyl acetoacetate with ethyl acrylate…

A: The key steps involved in this conversion are the abstraction of acidic proton by means of strong…

Q: The SN1-E1 solvolysis of the compound below would give substitution products that are H,O products…

A:

Q: Write the expected substitution product(s) for each reaction and predict the mechanism by which each…

A: The expected substitution product has to be written. The mechanism by which each product is formed…

Q: What is the major product of the following reaction sequence? D= deuterium, an isotope of hydrogen.…

A:

Q: For each reaction, give the expected substitution product and predict whether the mechanism will be…

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

Q: 1. Write the mechanisms of the following reactions and examine the products as stereoisomeric.…

A:

Q: a) H20 .CI Br2/H20 b)

A: The first part will follow the SN1 reaction. In this reaction, the good leaving group will leave by…

Q: Determine the mechanism of nucleophilic substitut a. Br + -CN acetone b. + -OCH3 C. + CH3OH Br H Br…

A:

Q: 4. Identify the carbocation intermediate for each substrate and then rank their reactivity towards…

A: SN1 is substitution nucleophile unimolecular reaction. The reactivity of SN1 reaction is depending…

Q: please show the detailed mechanism for each step for the reaction below. OTBDPS Me TMANO (anhydrous)…

A: Step 1 : alklyne addition to two coblat atoms. Step 2 : olefin addition to one of the coblat atom.…

Q: Identify the nucleophile that attacks the carbocation intermediate in the acid-catalyzed hydration…

A:

Q: er: HBr CH3 CHa CH2 CHa Br CH3 CH2 CH2 CH2 Br + Hao

A:

Q: Supply the missing reagents, intermediates, and final product in the following synthesis. OH A 1. B…

A: The above given series of the reactions includes various type of reagents which reacts with the…

Q: Draw the structures for the intermediates and product C, D, and E (only) in the following synthesis.…

A: Step 1 : LAH reduction of propinoyl chloride gives n-propanol. Step 2 : n-propanol is subjected to…

Q: 2.) Rank the following in order of increasing nucleophilicity, Place the appropriate letter on the…

A: the answer is as follows:

Q: CI H3C ELOH, NaCN Br H3C DMF ÇI Na H;C CH3 éter

A: There are two types of nucleophilic substitution reactions. Unimolecular and bimolecular.

Q: Draw the coupling product of the Pd(0)-catalyzed Suzuki reaction between the compounds shown. Show…

A: coupling reactions :          When two substrates are combined in the presence of a metal catalyst,…

Q: Determine the mechanism of nucleophilic substitution of attached reactionand draw the products,…

A: In the given reaction, the SN1 nucleophilic substitution reaction will occur. The first step…

Q: Provide the product and mechanism for the following reaction: C12 (1 equivalent), AIBN, heat 2. 3.…

A: Step by step mechanism is explained.

Q: (d) 1) LİAIH, H2N- 2) H,0*

A: LiAlH4 reduces amides into amines .

Q: (iii) Draw the organic products of the following Pd-catalysed reactions, paying particular attention…

A:

Q: T, SiazeH/THF 2. Naoti, A2oz Hzo H aldohyde pentanal

A: We have to give the mechanism of the given reaction.

Q: CO7T14Q0667 Give the major elimination product of the following reaction. Br ? (CH3)3COK NH2 OMe…

A: in elimination reaction one group is eliminated and new pie bond is formed.

Q: Predict the product and provide a detailed mechanism. Bu,SnCl (0.1 eq) NaBH4 (1.2 eq) hv…

A: Introduction: For a good radical coupling reaction, a mixture of tertiary butyl tin chloride and…

Q: What is the major product for the reaction sequence and the substrate shown? 1. NANH, in NH, A 2.…

A:

Q: Draw the organic products of the following Pd-catalysed reactions, paying particular attention to…

A:

Q: Draw the products of the following ozonolysis reactions: O, ? + ? (1) Me,s Os ? + ? (2) Zn, HCI

A: Reaction in which addition of oxygen or removal hydrogen takes place are called oxidation reaction.…

Q: List the following in increasing order of nucleophilic strength.…

A: Kindly get the answer given below.

Q: 5. Arrange the following species in order of increasing nucleophilicity: CH3CH2S-, CH3CH2O¯,…

A: • Good Nucleophile has the following characterstics:-(i) Domon atom less Electronagative.(ii) Amion…

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.