p) Circle the major product for the following reaction. CH,CH,CI O,N- H2 AICI; O2N- O2N- H2 H2 II O,N- O2N- H2 H2 II IV

Q: SCH, (a) H3C" CH3 OCH3 (b) H3C CH3 OCH3 Br (с) OCH3 ČH3 ČH3

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Q: Which bases can be used for an E2 reaction that follows Hofmann's rule? Choose all that apply. O…

A: According to Hoffman rule, an elimination reaction occurs to produce less substituted alkene which…

Q: Ph. OTs OTs NaOH NANH, ? ? NaOH ? A В C Ph. CI NaOH dilute NaOH ? D

A:

Q: CH3 -CH3 KMN04 (warm, conc.) CH3 H

A: Oxidation of 3-methyl Hex-3-ene:

Q: 16.Draw in the curved arrows for the SN2 reaction shown. Oe 17. Draw in the curved arrows for the E2…

A:

Q: Draw curved arrows for the following reaction step. Arrow-pushing Instructions CH3 CH3 H-0-H H3C-C+…

A: This is SN1 reaction  When tertiary butyl chloride reacts with water forms carbocation and gives…

Q: Draw the major product of the following reaction and enter its InChI code in the space provided. OCH…

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

Q: Draw the major organic product of the reaction shown below.

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Q: Predict the Majar products of the reaction 1.Oraw MechanisM ( Label each arrow with its Dattern) Brz…

A: Electrophilic addition :- Addition of bromine to alkene is a type of electrophilic addition…

Q: appropriate H3C CH3 Br КО-+-Bu ID НО-+-Bu a. CH3 NaOEt b. Ph-c -Br CH3 c. Show the curved arrow…

A: In the two reaction, the first one is an elimination reaction. Second one is nucleophilic…

Q: OCH3 C-H C–H + H,O + ? OCH3

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Q: CH3 Na/CH3ОН NH3 (liquid)

A: Given reaction is example of birch reduction.

Q: 1. Show how to carry out the following transformation. N ? N.

A: Note: Bromination of benzene. Acetylation of bromo benzene. Azo coupling. Sonagashira coupling.…

Q: HO What sequence of reagents can be used to accomplish the con

A: Following are the steps to accomplish the transformation 1. Free radical substitution to give alkyl…

Q: the

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Q: HBr "SN1-like" H :0. :Br: H 2° alcohol 3° alkyl bromide

A: Given reaction follows Sn1 mechanism.

Q: CH3 + HBr CH=CH2 + HBr `CH3 HC=C¯ + D2O H2O -C=C-CH3 H2SO4

A: Given reactions,

Q: Select the product of the reaction sequence below. A B. Br Br HNO₂ Br₂ H₂ H₂SO4 FeBr, Pd/C NO₂ NO₂…

A: Benzene under go aromatic electrophilic substitution reactions.

Q: 'hich of the following reagent best accomplish this transformation below? -CH=CH- -CEC- A (1st)Br2,…

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Q: 5. The reaction below proceeds through a 4-step mechanism. Classify each step according to the…

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Q: Rxn involve cleavage of -H Na NaOH CH3CH,C-OH Na,CO3 + iii) Reduction i. LİA||1, CH;CH,C– OH ii.…

A: Introduction: Carboxylic acid: Carboxylic acid is an organic acid with general formula RCOOH. R can…

Q: 4. Which one of the following compounds will react faster by SN1? PhBr PhCH2Br PHCH= CHBr MezCBr…

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Q: Starting from intermediate X, complete the mechanism. Provide curved arrows for both steps and draw…

A: The carbocation formed in the intermediate X is unstable because it is present at bridge head…

Q: Which reaction A through D yields hexan-1-ol? Click on a letter A through D to answer. но 1. LIAIH4,…

A: Solution :    Organic reduction of carbonyl compounds taken place by a different reducing agent .…

Q: Circle the least reactive compound in an SN2 reaction. Explain your choice. H H. CH2I CH,CH,I

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

Q: Sometimes carbocation rearrangements can change the size of a ring. Draw a stepwise, detailed…

A: The -OH group of alcohol abstracts a proton (from acid) as shown below:

Q: Which SN1 reaction is each pair is faster? А. CI OH2 H20 .CI OH2 H20 CI В. H20 CI OH2 H20 OH2 B,

A: Unimolecular nucleophilic substitution reaction (SN1): This reaction proceeds into two steps. The…

Q: Use curved arrows to show how E is converted to F by a two-step reaction sequence consisting of a…

A: In sigmatropic rearrangement, the rearrangement of pi bond and the breaking of sigma bond take…

Q: What will be the major product of the shown E2 reaction: CH3 H3C-C-o CH3 acetonitrile H. Br…

A: The elimination reaction E2 is a bimolecular elimination, which has only one step. A new bond is…

Q: Propose a mecahism for the following reaction and include all relevent reagents (you may use any).…

A: This is a multi step synthesis reaction . By using the starting material with various reagents we…

Q: Draw the major organic product of the reaction shown below. HO- NaNH2 +

A: Given reaction is reaction between cyclopentanol and sodium amide.

Q: 2) Follow the flow of electrons indicated by the curved arroWs in the reaction and predict the…

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Q: CH3 CH3 CH3 CH3 CH3 H3C Y

A: Interpretation -  To complete the mechanism of the reaction starting from the intermediate  X, by…

Q: H2O, H2SO4 H9SO4 A. В. С. E. None of these choices is correct. D.

A: In presence of HgSO4 and H2SO4 , H2O ,oxymercuration-demercuration reaction is carried out and…

Q: Propose a plausible mechanism using curved arrows that shows the 10. formation of product A only.…

A: The organic reactions are carried out in more than one step. It is carried out with the help of…

Q: Draw the major product of the following reaction and enter its InChI code in the space provided.…

A:

Q: 2. Draw the complete, detailed El mechanism for the following reaction (including including curved…

A: Tertiary alkyl halide gives E1 elimination to form an alkene. The alkyl halide eliminates hydrogen…

Q: For the dehydrohalogenation (E2) reaction shown, draw the major organic product, including…

A: E2 reaction is a bimolecular elimination reaction to give an alkene. In the transition state, the…

Q: Draw a step wise, detailed mechanism for the following reaction.

A: To find: The detailed mechanism of the given reaction.

Q: For the reaction below provide all possible product(s), and circle the major product.

A: The question is based on the concept of organic reactions.   We have to identify the product formed…

Q: When 3-methylbutan-2-ol is treated with concentrated HBr, the major product is 2-bromo-…

A: The answer

Q: Choose the correct product of this reaction. H3C H3C. CH3 1. еxcess KMnО,NaOHwater 2. Н,О" H3C H3C…

A: Given : Reaction  To find : Product  Solution : when carbon atom directly attached to benzene ring…

Q: 4. Draw the appropriate Newman projection (you can just draw the 1 that matters when you determine…

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Q: s. What is the main product of the reaction shown in the box? CH3 H2, Pd (cat.) ? CH3 CH3 -CH3 M CH3…

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Q: 9. Draw a complete, detailed mechanism for the reaction below, and product(s). CH,OH NaOCH3

A: Ester are derived from substitution reaction of carboxylic acid and an alcohol, they are volatile…

Q: Select the arrow drawing that best describes this step of an E1 reaction. H I-0: І H3C I нн i 1-0:…

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Q: Add curved arrow(s) to draw the final step of the mechanism. 18rt Br 3-3 CH₂ H₂C Br H₂C

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Q: Which reaction does not correctly circle the more stable base? A) + CH3 B) + OCH3 OCH3 C) Но + H20 +…

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Q: Which, reagent combination will achieve this transformation? CN Ho но- A) 1) HBr 2) NaCN 3) H20 B)…

A: we are given an unsymmetric alkene as the reactant. We have to add -CN to the least substituted C of…