Amidificationreaction • CH NH, k Amide Acid. Hydrolysis reaction • HOH+ HCI NH2 1. Amide Base Hydrolysis: CH,CH,CH,-C-NH-CH3 + NaOH 2. Draw in the space below the hemi and acetal formed in the following reaction. (include all products) CH,-CH,-C-H 2 CHy-OH > hemi acetal:

Q: Which of the following statements about ethanethiol (CH3CH2SH) is(are) correct? Ethanethiol will be…

A: Ethanethiol in presence of NaOH: CH3CH2SH+NaOH→CH3CH2S-+Na++H2OEthanethiol…

Q: What is the charge of domoic acid at a pH = 1? (a) -1 (b) 0 (c) +1 (d) +2 (28)What are the the…

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Q: CH;-0-C- methyl cyclopentancarboxylate O methyl cyclobutancarboxylate O ethyl cyclopentancarboxylate…

A: Using rules of IUPAC nomenclature we can name given compounds.

Q: Which reagent will convert pent-2-yne to pent-2,3-dione.?     KMnO4, neutral and aqueous     1)…

A: Answer

Q: CHO NaBlty -> MEOH Primary Alc. Secondary Alc P Aldehyde - Ketone I Tertiany Ale. - Carbox ylic Acid

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Q: OTMS OTMS OH "MgBr /Br OH OTMS ICH,OH CH2OH B- TMS-CI/pyridine C- MgBr2/ether A- TMS-OH/pydidine E-…

A: In the given compound bromine and alcohol groups are present. The bromine substituent reacts with…

Q: 1-Ethyl-2-methyl-cyclopent-1-ene plus 1) O3, -78 °C; 2) (CH3)2S yields O Heptanoic acid and CO2…

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Q: Draw the major product of this reaction. Ignore inorganic byproducts and the amine side product. N'…

A: Amide is a carboxylic acid derivative and it converts back into carboxylic acid by reaction with…

Q: e Br KOHEIOH A 32 THF NaCN DMSO NaOH H₂O, reflux CH₂CH₂OH CH₂CH₂SNa

A: The products of the above reactions are shown below.

Q: Afatoxin B1 is one of the most potent carcinogens known. Which carbon on the structure is an acetal?…

A: The given compound is the  structure  of Afatoxin B1  which is  one of the most percent carcinogens…

Q: Given this retrosynthetic analysis, show how meclizine can be synthesized from the four named…

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Q: Draw the major product of this reaction. Ignore inorganic byproducts and the amine side product. N'…

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Q: II AICI3 V 1) O3 II (H+], CH;NH2 NABH3CN (C10H12) 2) DMS (C3H1,0) (C10H15N) -H20 1) EtMgBr 2) H20 IV…

A: Details mechanism are shown in image.  The IV compound is : 3-Phenylpentan-3-ol Hence the correct…

Q: How would you convert benzoic acid (C6H5CO2H) to each compound?

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Q: Use the malonic ester synthesis to prepare each carboxylic acid. .COOH a. CH;CH,CH2CH¿CH¿CH2COOH b.…

A: Malonic ester is an dicaebonyl compound in which -CH2 group is sandwitched between -CO2Et group.…

Q: 1. LDA CH2CH3 2. CH3CH2CI 2-Chloro-1-phenylpropanone 1-Phenylbutan-1-one…

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

Q: (a) Circle the two compounds that are not carboxylic acid derivatives. Circle only two. CONHCH NOH…

A: A. Carboxylic acid derivatives are : ester, amide, nitrile, anhydride, acid chloride etc.  But…

Q: Show how to prepare pentanoic acid from each compound. Q.) 1-Pentene

A: Alkenes are unsaturated hydrocarbons with their general formula- CnH2n . Alkenes have one double…

Q: g. formyl chloride + 2 equivalences of methyl amine H-C = Cl; -) H-c-ci: -7 H- NH2 N-CHy CHy H- Br.…

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Q: Arrange the following compounds in order of decreasing acidity.CH3COOH CH3OH CH3CH3 CH3SO3H CH3NH2…

A: The acid strength is the ability of the acid, symbolized by the chemical formula HA, to dissolve…

Q: 1. Nai, ethanal a) Cyclohexanecarbaldehyde 2 H b.) Sodium Flouride + 3-iodo-3-methylpentane (hìnt:…

A: when NaBH4 is added to aldehyde , then it change the aldehyde group to alcohol group. NaBH4 is a…

Q: Rank the following in order of increasing acidity. CH3COOH CH3CH2OH2* CH2FCOO H2O H2SO4 CHF2COOH

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Q: Hw! -bromotoluene + NaNH, NM, () ® CH₂ NH₂ o-toluldine direct-substitution product CH3 -NH₂…

A: Initially NaNH2 will react with liq NH3 to form NH2-  NaNH2 + NH3(liq) →NH2-

Q: Q7:- Which compound has the highest boiling point Acetic acid or Propan-1-ol ? Why ? How can orenare…

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

Q: k) 4Heptanone (ENH -HO 1) Acetaldehyde +1 MENH NABH CN HeSOwHSO. m) MeC CH HO 1) 9-BBN 2) HO. "OH 1)…

A: In this question ( k, l and m ) we will draw the Product of the Reaction, Reagent and starting…

Q: acetaldehyde dropwise NaOEt/EtOH NaOH, ETOH, H2O CI CI 1) NaOEt. EtOH (xs) Br(CH2)4Br OEt 2) NaOH,…

A: These are the examples of Aldol condensation and alkynation of active methylene compounds.

Q: Rank the following alcohols from strongest to weakest acid: CCl3CH2OH   CH2ClCH2OH    CHCl2CH2OH

A: Strong acid has higher acid dissociation constant, whereas weak acid has lower acid dissociation…

Q: Draw the product of the following reaction:

A: When reaction occurs between primary amine and a carbonyl compound (aldehyde or ketone), imine is…

Q: a) b) CH, н — с- с — н с — сн, — Сн, C H H Alcohols (alkanols) - hydroxyl ketones - carbonyl c) H (P…

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Q: Devise a 5-step synthesis of the carboxylic acid from acetylene. 1. reagent 1 2. reagent 2 3.…

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Q: Draw the major product of this reaction. Ignore inorganic byproducts and the amine side product. N'…

A: Given reaction is :  Draw the major product of the reaction = ?

Q: Pronde structure tor 6)-tert-butyl2amino-3- thiopropanoate; thio = -SH Tdentify all procuk forme whe…

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Q: LE and Consider the dehydration of 2-propanol in sulfuric acid: H OH H H- -C -C-C-H H₂SO4 H H H Draw…

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Q: Name and draw the products of each reaction. (a) 1-propanol + hydrobromic acid - HS0, (b) 1-pentanol…

A: a.) The reaction of primary alcohols with HBr results in the formation of substitution product. The…

Q: What alkyl halide is needed to prepare each 1° amine by the Gabriel synthesis?

A: Gabriel phthalimide synthesis is used for the preparation of primary amines from primary alkyl…

Q: носн-CH,он, НА Mg, Et,0 4-Bromobutanal ► A (CgH,,O¿Br) [B (CgH;;M9O2B1)] (1) CH,CHO CH,OH (2) H,O“,…

A: Aldehyde is one of the important functional group in organic chemistry. Protecting group strategy is…

Q: JU PAC ndme for Hhe follwing Melecole? lwhat is the 1UPAC neme OH H. 1. 3-Ethyl- 5-hydronyhexenal 2.…

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Q: How would you convert benzoic acid (C6H5CO2H) to each compound?

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Q: 1. p-toluenesulfonyl chloride CH;CHCH,CH2OH 2. ČH3 CH;CH,OH HCI, . + CH;CH `H excess

A: Reagents are the chemical substances that are required in the route of chemical synthesis to convert…

Q: OH Br₂ dil. HNO3 acetic anhydride KOH HCI/Fe n-BuBr acetic anhydride

A: We have to complete the following reaction pathways with phenol.

Q: halide with H2O? benzyl alcohol Ph;COH cydohexanol (CH3)CHOH 1-propanol A B D E

A: Unimolecular nucleophilic substitution (SN1) reaction proceeds via formation of carbocation…

Q: C4H8O2 + SOCl2 -- > ? (The product of butyric acid + thionyl chloride?)

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

Q: You have an alkyl halide and the product has a thiol group without an alkyl, what is the reagant?…

A: These are substitution  reaction which takes place between alkyl halide and Nucleophile

Q: but-2-en-1-ol + but-2-enoic acid, CH3CH=CH-COOH. eq. NaOCI TEMPO 1 PCC NAOCI T MeD.

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Q: Q6:- Rank the following substances in order of increasing acidity , Justify your choice.…

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Q: Show how to convert 4-methoxybenzyl chloride to each amine.

A: Here, the product is a primary amine. As it has only 1 carbon atom directly attached to the…

Q: In the chapter, we stated that the imine in this reaction is reduced. Verify that this is the case…

A: In the imine reduction, there are two electrons involved. The electrons from the NaBH​​​4​​ are…

Q: Q1. Name parts a through d - draw parts e through h: CH; — CH—CH —СН-—NH> ČH3 а. b. .CH3 N. H3CH2C…

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Q: он CH3 -CH2-CH-CH2-CH-COOH (a) 4-hydroxy-2-methyl-5-phenolpentanoic acid (d)…

A: We have to write the IUPAC name for the given following compound.

Q: What products are formed when the amine below reacts with HC1? CH,CH,CH,-N- CH,CH,CH,CH,CH,CH, A)…

A: Correct Option :    B)  CH3CH2CH2-N+H2-CH2CH2CH2CH2CH2CH3              +    Cl-

Amines

Amines are organic compounds with a nitrogen atom having a lone pair of electrons on it. They are derived from ammonia (NH3) wherein hydrogen atoms are substituted by an aryl or alkyl group.