1. Give the type of reaction, mechanism with curved arrows, and products for the reaction below: Br `NH2 100 °C

Q: Draw a mechanism to explaim the observation show the movement of electrons with a cwwwed w Draw all…

A: In the given process,  formation of electrophile is quite important, which proceeds the further…

Q: 5) CHO CH,OH + NABH, + 4 H,0 + H,BO, + NAOH OCH OCH, Vanillin Vanillyl alcohol a) For the above…

A: The given reaction is a reduction reaction. Due to the mild reducing properties of the NaBH4, it…

Q: 3.3 Explain the reasons why the reactions provided below DO NOT work and show the other expected…

A: Reasons: a.  The initial reaction will not work because nitrogen of aniline will react fast with…

Q: What is the most proper major product for this reaction scheme? 2. 2. 1. 2CH,MgBr, THF 2. H D O A

A: Acid chlorides react with two equivalent of Grignard reagents to produce tertiary alcohols. Because…

Q: Select the starting material for the reaction shown. 1. NaBH OH 2. H20 JDHDMC OH

A: Sodium Borohydride can reduce aldehyde and ketone but not the corboxylic acid, esters, amides.

Q: 8. The first reaction below gives a mixture of two products, while the second reaction is completely…

A: The formation of different kind carbocations in the chemical reaction are shown below.

Q: Give the major product of the following reaction. Br2 (1 mole) FeBr3 Br Br Br Br Br Br There is no…

A: The given reactant ethylbenzene reacts with bromine in the presence of iron bromide is called…

Q: Question attached

A: The given reaction is:

Q: Identify the product(s) of the reaction below. hv ? NBS Br Br Br Br

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: Draw the structure for the transition state in each reaction. а. OH2 H20 b. HO, -OH H20

A: Each chemical transformation passes through an unstable and not isolable structure called the…

Q: Cl2 uv or heat

A: In presence of sunlight at alpha position cholorination take place

Q: 8. Consider the reaction below to answer the following questions... Br KI H3C. H3C IBr CH3 1 2 a.…

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Q: 6. Give the maior product br the follawing reaction CH3-CH-CH2CH 3.

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Q: 0. The following transformation would be considered a(n)? Br A) Reduction B) Oxidation C) Addition…

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Q: Which product would be formed in the reaction below? Brz ? H;O а. Br

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Q: Give the product(s) of the PINACOL rearrangement reaction shown below? OH H2SO4 HO

A: Given,

Q: 4. Given the reactions below, explain the limitations of the Gabriel synthesis. 1) KOH/CH;CH,OH KOH,…

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Q: 6. Predict the product(s) and provide the mechanism for each reaction below. _NaOCH, HCl catalyst…

A: Organic reactions.

Q: 6. Provide mechanisms for the reactions below. Pay attention to the type of arrows that you use. You…

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Q: Identify the reagents that will form the product in the reaction below. O a. HBr b. 1.…

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Q: The reaction of 2,2-dimethyl-1-propanol [(CH3)3CCH2OH], also known by the common name neopentyl…

A: Neopentyl alcohol is derived from neopentane. It has a prefix neo because of the presence of…

Q: The reaction of cyclopentyl bromide with sodium cyanide to give cyclopentyl cyanide roceeds faster…

A: The reaction of cyclopentyl bromide with sodium cyanide to give cyclopentyl cyanide proceeds faster…

Q: Br product 4 + 2 18 B .Br product 3 Br 7 3 product 2 + 5 00 product 1

A:

Q: 3. For each reaction below identify the electrophile and the nucleophile. Na + CH,CI CH,N3 a. NO,…

A: A Nucleophile Is A Reactant That Provides A Pair Of Electrons To Form A New Covalent Bond.  And  An…

Q: Identify the major product that would be produced in this reaction. NAOCH, Br Br NaOCH, H,0* heat HO…

A: Carbonyl compound is present in the presence of acid or base then formation of enol and enolate will…

Q: H,C + CH3 H,C

A: First reaction is simple ester synthesis Second reaction is not favourable

Q: (b) Write out the product(s) for the reactions below. Analyze the compounds (i) and (ii) below and…

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Q: 34. Which molecule is the most reactive in an S2 reaction? (A) CH,CH,CH,a (B) CH,CH,CH,OH (C)…

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Q: Choose the product most likely to form during the sigmatropic rearrangement shown below: - O A O B

A: Sigma trophic rearrangement:  The rearrangement reaction in which a sigma-bonded atom or group…

Q: 5. For each reaction below, please fill in what is missing in each box. For reagents, more than one…

A: Friedel-Crafts Alkylation reaction is the reaction of benzene with haloalkanes in presence of…

Q: Select the most likely product produced From this sequence of reactions - N NH soclz LAH You H.

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

Q: 5. Write the stepwise mechanism for the reactions given below. Show all electron flow by using…

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Q: Give the major product of the following reaction. O,N - ? H30* S-OH O,N NO2 O,N- NO, NO2 NO2 O,N-…

A: The species sulphonic acid is get rid of the benzene ring in the sight of the species acid along…

Q: 1. Predict the major product at 20 °C and explain why this given product is favored. Is this…

A: The kinetically favored product and thermodynamically favored product is formed at low temperature…

Q: 2. Write a complete mechanism for the reaction shown below. Show all steps and electron- pushing…

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Q: What is the most likely first step of this reaction's mechanism? CH3 CH;CH2OH Br

A: The reaction given is SN2 reaction in which the nucleophile attacks and removes the leaving group.…

Q: 3) For each reaction below, indicate which starting material is the Nucleophile and which is the…

A: Electrophile:                      It is an atom or ion or a molecule that have a tendency to be…

Q: Predict the most likely mechanism for the reaction shown below. CI CH₂ CH3 H₂O A

A: The following mechanism are as follow.

Q: h of the following reactions would provide the best yield of this compound? NO2 NO2

A: Pericyclic reactions occur under thermal or photochemical condition. These reactions do not require…

Q: Determine the product for each reaction. HBr -FE OCHCH, 6. CH 1) CH,CH,O Na HOW OCH,CH, DCHCH, C H…

A: Epoxide ring opening reaction takes place when treated with nucleophiles. Ring opening reduces the…

Q: 3-The reaction of 2,2-dimethyl-1-propanol with HBr is very slow and gives 2-Bromo-2-methyl butane as…

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Q: What is the major product of this reaction? N-H Catalytic H+ EH20) 8.3.8.8 HO, 'N. NH2 но N- (a) (b)…

A: Answer:- This question is answered by using the simple concept of chemical reaction of ketone with…

Q: What is the major product when the reaction shown below is carried out at low temperatures? H-Br ?…

A: If the reaction is carried out at low temperature then kinetically controlled product is obtained to…

Q: 1) МezNH 2) НСНО, H* 3) CH3I 4) Он-

A: The reaction is the shift base formation.

Q: 6. Provide reasonable mechanisms for the conversions below. -CH30 CH CH, 1. heat 2. NaOH H,C. CHs

A: There is (4+2) cycloaddition reaction .This is Diels alder reaction.

Q: 4. Supply the missing reagent/reaction conditions required to complete the transformations shown…

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Q: 8) Draw the product of the Sn2 reaction illustrated below. Comment on the stereochemistry of the…

A: 8. Given reaction,

Q: Choose the best reagent(s) for carrying out the conversion of the reaction below: CH-CH-CHCH,cоон…

A: Since, you have asking multiple questions so I will solved first question for you  You can see the…