CH-CH, CHCI, Show the mechanism step by step to obtain the product

Q: Using curved arrows, please give the mechanism for the following reactions. MEOH -Br LDA DIPA

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Q: Propose a mechanism for the following reaction. (Hint: Number the carbons to help you see where they…

A: The mechanism is as given below:

Q: The following reactions give two different products. Shows the mechanism leading to their formation.…

A: For the ring opening of epoxide there is a rule ,  1) When the reaction is performed in the…

Q: Identify the nucleophile and leaving group and draw the products of each substitution reaction.

A: Nucleophilic reaction : In a organic reaction when an electron rich compound (nucleophile) will…

Q: CH,OH /H° ОН ANISM

A: - given compound is the carboxylic acid  Which reacts with the alcohol in presence of acidic…

Q: Please give the product and the mechanism of the following reaction. NaOH -H Br H2O H II

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

Q: Provide reagents and conditions with mechanisms to produce the products indicated. HO OH o-CH3 HO OH…

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Q: H3CO. NaOH + H;CO H3CO OCH3

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Q: Complete the following reaction and propose a mechanism.

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Q: Give the product and mechanism for the following reaction. I. LIAIH, 2. H,0 CI

A: LiAlH4 is the strongest reducing agent. It will reduce aldehyde , ketone, corboxylic acid ,acid…

Q: + Naz BOz NABHY (CH3)2CHOH

A: NaBH4 is a reducing agent that can reduce aldehydes and ketones.

Q: H,O + Br2

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Q: Predict the major product and show the complete mechanism for each electrophilicreaction below.

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Q: Propose a mechanism for the following transformation, SHOW ALL BOND-FORMING AND BOND-BREAKING STEPS.…

A: Carbonyl proton gets protonated to produce oxonium ion. Intramolecular nucleophilic attack by…

Q: 3) Complete the following reaction OH A) B) OH Br Br₂, H₂O OH | CH3 OH H OH OH CH3 11H Br Name 3…

A: Addition of halogen , first for transition state as  cyclic halonium ion then converted into product…

Q: HO. CH2-NEN: + N2 (CH, =R=R)

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Q: CO,Me MeOH H;O+ Br

A: Synthetic organic chemistry involves the conversion of the reactants into the appropriate products…

Q: Propose a mechanism for each reaction, showing explicitly how the observed mixtures of products are…

A: Mechanism for (a) has to be given below, (a) 3@methylbut@2@en@1@ol + HBr S 1@bromo@3@methylbut@2@ene…

Q: c) Propose a mechanism for the following reactions. OH o BrMg MgBr HO ii) H20

A: Organic reaction mechanisms: Reaction of anhydride with Grignards reagent.

Q: Propose a mechanism for this reaction. CICH,CH,OH Na,CO, H,0 H,C-CH,

A: Given reaction,

Q: 2. Indicate reagents or conditions for the following transformations involving rearrangements.…

A: As per the rules only first three question can be answered.

Q: CH3 *NH, H.

A: Sunthesis:

Q: TSOH MeOH

A: Product for the given reaction is,

Q: Propose a mechanism for each reaction. (а) + H3C НО ОН CH3 HO H,SO, (b) Ph С—ОН Ph Ph Ph

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

Q: mechanism

A: 1- NaH, THF  2- Bn-Cl ( benzyl chloride ) = C6H5-CH2-Cl 3- LiAlH4

Q: Predict the major product and show the complete mechanism for each electrophilic reaction below. (a)…

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Q: CH H;SO, HO- CH

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Q: dicate the steps for the transformation HO. HO, → → → H5C6 OH

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Q: Provide the mechanism and the product for the following reaction: Br* MeOH

A: A species having a positive charge is known as the electrophile whereas the species having electron…

Q: Propose a step-by-step mechanism

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Q: Show how to bring about the following conversion. CH,O CH3O

A: The product is the result of Michael addition to an alpha-Beta-unsaturated ketone followed by…

Q: he following reactions give two different products. Show the mechanisms leading to their formation.…

A: As CH3OH is weak nucleophile and CH3O- is strong nucleophile In first reaction the reaction takes…

Q: Propose a mechanism for the following reaction CH CH CH OCH;CH; 1. CH,CH,0 2. CH,CH CH,CH,

A: Given reaction,

Q: Perform the following transformation and propose a mechanism Br ОН Br НО

A: When alpha-bromo ketone reacts with NaOH then to get carboxylic acid is formed. This is called…

Q: SHOW THE MECHANISM AND STEPS: Benzene---> Propiophenone(C9H10O)----> Methanol

A: The first step of conversion from the benzene to propiophenone take place by acylation reaction

Q: H3CO, NaOH H,CO H3CO OCH3

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Q: *NH H*

A: Reactants are secondary amine and ketone, medium of reaction is acidic medium.

Q: Could u show the products and the mechanism of the following reaction and give a short explenation?…

A: No, there is not possible to form product by elemental bromine instead of acidic HBr because…

Q: Predict the product of the first and third steps and propose a mechanism for all three steps. Br2…

A: In the first step, the Br2 will be attacked by the alkene and form a 3 member ring intermediate. Now…

Q: Provide reagents and conditions with mechanisms to produce the products indicated. HO OH o-CH3 OH OH…

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Q: Propose a mechanism for the following reaction:

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Q: 5. Using curved arrows, showing key intermediates and any formal charges, propose a detailed…

A: Epoxide ring opening can take place in either side of ring which depends on the condition of the…

Q: 3.( ) Propose an appropriately-detailed electronic mechanism that accounts for the reaction below:…

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Q: он ONa 1. CO, A, P 2. H,SO, NaOH -HO-

A: The given reaction is the synthesis of salicylic acid from phenol which can be represented as;…

Q: MEOH H;O+ Br

A: The above reaction may be proceed through the given mechanism-

Q: a) Complete the following reactions: (i) H;C-C-Ci + H2O A + B HO H;C. CH3 SOCI, + D + so, (iii) H;O*…

A: Introduction : We have to make the products for the following. As per company norms we can not…

Q: Choose the mechanism that forms the main product of the following reaction. Er ONa CH3CHOH calor

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Q: 4. Suggest a detailed mechanism for each of the followir reactions: CH, (a) H;SO. C-CH, CH, 0=C-CH,…

A: Since you have asked a question with multiple sub-parts, we will solve first three subparts for you,…

Aromatic Compounds

Aromatic organic compound or aromatic system is an important class of hydrocarbons under the branch of organic chemistry. Aromatic compounds are also called arenas. The definition of aromatic organic compounds can be stated as a class of organic compounds with a planar cyclic ring of atoms bonded through alternated single and double bonds. Due to these alternating bonds, a peculiar feature termed as ‘resonance’, that is, delocalization of pi electrons or the electrons is shared within the atoms of the ring which are present in the aromatic compounds. The word ‘aromatic’ includes a Greek word ‘aroma’ which means smell, indicating that they were named as such due to the sweet odor they produce. Many well-known flavors such as vanilla, cinnamon, and few scents from flowers are extracted from aromatic compounds. Benzene with chemical formula C6H6 is a very common aromatic compound that contains six atoms of carbon held in the cyclic ring of alternate double bonds. It is also to be noted that not all aromatic compounds contain benzene ring. This can be explained by Huckel’s rule.