Rank the following alkyl halides in order of increasing SyI reactivity. Br Br B: Br C: А: A B C Least Reactive Most Reactive

Q: What is the major product for the following reaction (A) (B) CH3CH₂CH₂CH₂Cl AlCl3 (C) (D)

A: The given reaction is Friedel craft alkylation in which aromatic proton replace with alkyl group.…

Q: 10. NBS KOBr (A) . Product (A) is : LOH HO- NH (a) (b) (c) (d) -NH2 - NH2

A: This reaction is Hoffmann Bromamide name reaction and  intermediate is 'nitrene'.

Q: 1. Rank the following alkenes in order of increased stability. 2 5

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Q: H. CI H. HOE HO, HO, H. Br HO. CI

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Q: 1. CH3-0- CH;O-ċ-CH2-ċ-OCH3 2. CH3-Br 3. НСИН-0, А

A: ->CH3O^- is base which can abstract most acidic hydrogen.

Q: (b) Show a plausible mechanism (including all steps with proper arrow pushing) to explain how the…

A: Usually, in organic reactions, ring expansion occurs when there is a chance to get converted into a…

Q: 1 / 1 100% 1. Draw the major expected organic product for the following reaction: excess CrO3, H3O*…

A: The given reaction is a Jones reagent ia powerful oxidising agent which oxidised aldehyde as well as…

Q: Explain why the following bromoketone forms different bicyclic compounds under different reaction…

A: Given reaction,

Q: Explain why α-pyrone reacts with Br2 to yield a substitution product (like benzene does), rather…

A: The given compound is aromatic as it involves delocalization of π-electrons as follows,

Q: Rank the following alkenes in terms of increasing stability. (A) (B) (C) OC<A<B OA< C < B OA < B < C…

A: Stability of the alkenes increases on increasing the substitution which means highly substituted…

Q: Vhich of the following pairs of compounds would you choose as starting materials for the synthesis…

A: The grignard reaction undergoes nucleophilic addition reaction reaction with the carbonyl compound…

Q: Rank the organic halides in each group in order of increasing SN1 reactivity. Br Br Br Br b. Br a.

A: Nucleophilic substitution reaction is the one in which a nucleophile replaces the leaving group. So…

Q: Rank the following carbocations in order of increasing stability. + CH,CH,CH2CH2CH=CH b.…

A: To rank the given carbocation in the order of increasing stability.

Q: Rank the organic halides in each group in order of increasing S2 reactivity. Br Br а. Br b. Br Br Br

A: Nucleophilic substitution reactions SN2 are those reactions in those reactions in which the rate of…

Q: What product will be obtained for the below reaction: RCH3 -? H3C-C=CH, I CI CH3 CH3 (A)…

A: The given organic compound, 2-methylpropene will react with ICl via an electrophilic addition of…

Q: 1. Draw the product of the following reactions: ether a) Br + Mg 1) ether b) + product of a) 2) H3O+…

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Q: What products are formed from reaction of one mole HCI with this ether ? (Hint: CI is a weak…

A: The ether is the organic compound formed by the combination of two alcohol molecules. The…

Q: Rank the fallowing compounds by everall energy. A o ccur the fartent via elimination - addition.…

A:

Q: Name the following alkyl halides: (a) Hзс Br Br CH3 (b) I (c) Br çI CH3 CH3CHCHCHCH,ČHCH3…

A: Since you have posted a question with multiple subparts, we will solve the first three subparts for…

Q: identify both products A and B in the scheme below. но CI-S-CH3 .. K O'Bu A В

A: Given reaction:

Q: Question 5

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Q: (а) -C- -ОН (b) -0-CH3 (c) -CI (d) C-CH3 (е) -NH3

A: Answer:- This question is answered by using the simple concept of effect of substituent on the…

Q: How many distinct (total) alkene products are possible when the alkyl iodide below under E2…

A: Elimination reaction :

Q: CH3 *CH cH2 || C A. B

A: Ans is C

Q: Rank the following alkyl chlorides below in terms of increasing reactivity with a nucleophile via…

A: We have to arrange alkyl halides in order of increasing reactivity in SN2 reaction.

Q: но NBS HBr CCI, ether а. b.

A: -&gt;HBr give substitution reaction . -&gt;NBS/CCl4 used for alpha bromination.

Q: A. Draw the acceptable major product for the following reaction H,SO4 Н-ОН Н-ОН H* H,0 H,SO4 H,O

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Q: Rank the following alkenes in order of increasing stability (least to most stable) I II III IV

A: A question based on alkene, which is to be accomplished.

Q: CH,C-CH,CH,C-H 32. The most probable product expected from the reaction of is: with one mole of HCN…

A: To Solve this problem we will complete the given reaction .

Q: aw the appropriate number of hydrogens on nitrogen and oxygen, where applicable. Draw product C. NH2…

A: Solution- Above given organic compound main product drawn below-   (c)-

Q: 1. Predict the major product(s) for these reactions: b. OTs CH;OH с. KMnОд, NaOH (аq) cold

A: The major product(s) for these reactions are

Q: A. Give the most stable enol form: 1. 2. C. Give the starting material/s that would provide the a,ß-…

A: We have given two ketone molecule and we have to give the most stable enol form and give the…

Q: Identify the reagents X in the following scheme O NABH4 with H30+ O KMN04 with H30+ All are correct…

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Q: Name each epoxide: CH3 a. b. C. (two ways) (two ways) CH Provide a systematic name for each of the…

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Q: 1 eq HI -78°C coldkinctb

A: 1- We know about that, at low temperature ( -78°C ) molecules reacting with each others with slow…

Q: a) CI H b) .N.

A: Concept is based on aromatic electrophilic substitution reactions.

Q: 2) order of decreasing reactivity toward electrophilic aromdticC cubstitution NH3 (2) 3)

A: We have to tell about the order for reactivity of electrophilic aromatic substitution .

Q: Rank the molecules A to D shown below by decreasing reactivity towards iodo cyclohexane. H;C-CH,OH…

A: Correct option is 2 . B &gt; A &gt; C &gt; D. B trifluoro ethanol is more acidic means more reactive…

Q: Assuming that the nitrogen in enamine is sp? hybridized, explain why the double bond of an enamine…

A: We have to tell why the double bond of the enamine is more nucleophilic then a typical alkene double…

Q: Arrange the following alkyl halide in order of increasing E1/ E2reactivity:

A: Elimination reaction occurs either via E1 mechanism or E2 mechanism. E1 mechanism occurs via 2 step…

Q: OH OH OH II III

A:

Q: CH3-Br

A: In this question, we will draw the major product.  You can see details mechanism and major product…

Q: Arrange the compounds in each set-in order of decreasing reactivity (fastest to s toward…

A: As you have posted question with multiple subparts, we will answer the first three subparts for you.…

Q: Two products are formed when methylenecyclohexane reacts with NBS? Show how each is formed.…

A: N-Bromosuccinimide (NBS) is a reagent used for the bromination of allylic hydrogen atoms.…

Q: Drawing Hydrohalogenation with a Carbocation RearrangementDraw a stepwise mechanism for the…

A: Hydrohalogenation: The addition of HX (haloacids) on carbon double bond is called hydrohalogenation.…

Q: What product will be obtained for the below reaction: ÇH3 -? H3C-Ċ=CH2 I-CI CH3 CH3 (A) H;C-C-CH,-CI…

A: When 2 - methyl propene , which is an alkene is treated with iodine monochloride , then Reaction is…

Q: Draw the structure(s) of the major organic product(s) of the following reaction. CrO3 / H30*

A: The given reactant is a ketone. The reagent used is an oxidising agent. Ketones are resistant to…

Q: The answer choices for part b ["How would you convert the alkene to a epoxide?"] are: (a) Br2/NaNH2…

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Q: 4. Identify the position where electrophilic aromatic substitution is most favorable. * HN' CH3 CH3…

A: EWGs are meta directing whereas EDGs are ortho para directing.