1. Synthesis of Aldehydes: A. B. C. Oxidation of 1° alcohol to an aldehyde Reagents: (i) Pyridinium chlorochromate (PCC)- Shop et ex epidehode Reagents: (ii) Dess-Martin Periodinane; CH₂Cl₂ Ozonolysis of Alkenes to aldehydes/ketones Reagents: 03; then Zn, H3O+

Q: Provide a detailed mechanism for the reaction shown below. Br2/H20 HO Br

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Q: 3. Synthesize each compound from ethyl acetoacetate. You may use any other organic or inorganic…

A: Active methylene group of ethyl acetoacetate can be alkylated with alkyl halide in the presence of…

Q: Give the IUPAC name for the following alkenes. Include an E/Z designation where appropriate. Part 1…

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Q: Consider the reaction scheme shown below. HCI [1] HO. (a) Provide a detailed mechanism for reaction…

A: This reaction will occur via 3 step. In first step protonation then Water molecule eliminate to…

Q: Br HI (1 eq.),

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Q: Write a mechanism that accounts for the formation of ethyl isopropyl ether as one of the products in…

A: When an alkene reacts with acid like HX then first it get protonated then X- attack to carbocation…

Q: Give the reaction conditions which could be used to bring about the transformation shown in two…

A: Oxidation and reduction are the key steps here. These steps will result in our desired product.

Q: 3. Suggest synthesis routes for the following conversions. Include brief reaction conditions.

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Q: Predict the product(s) for each of the following organic reactions. Draw the structure, but do not…

A: Given reactions are:

Q: Complete the Reaction below and provide the following (i) a detailed stepwise mechanism to account…

A: When ketones react with primary amine they form imines.

Q: Choose the best reagents to complete the reaction shown below.

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Q: 2) Provide a synthesis for the product shown below given the starting material. ОН ОН

A: By observing the starting material and the product, we can see both the reactant and product are…

Q: Give the IUPAC name for the following alkenes. Include an E/Z designation where appropriate. Part 1…

A: IUPAC priority order function group > multiple bond > substitutent

Q: 7В. (2' Draw the structure of the product, substrate or condition in the following reactions (should…

A: Alkene are unsaturated hydrocarbons. They have free electron density to give. thus it can easily…

Q: The reaction is a nucleophilic substitution, A is OH- and B is an alkyl bromide. Give the reaction…

A: The nucleophilic substitution reaction of alkyl bromide with OH- is given below

Q: a. H. Br OH Ph Ph "P HO

A: a. (i) Acid catalyzed amide hydrolysis. (ii) Acid FG to alcohol FG using LAH. (iii) Alcohol FG to…

Q: Thank you for the explanation, can you provide the IUPAC of both products please?

A: The important rules for IUPAC nomenclature of organic compounds:-Select the parent chain with the…

Q: Compound A Compound F HCI CH3OH H₂SO4 Compound B CH3 CH₂ CH₂ Cl Compound E NaOH K₂Cr₂O7 H₂SO4…

A: To forecast the results of electrophilic additions to asymmetrical alkenes or alkynes, organic…

Q: H2SO4

A: Here first OH gets Proton from H2so4 then rearrangement occur followed by elimination.

Q: ways ma starting materials and reagents. a cuprate an alkene an alkyne an alkyne

A: The given reaction involves the synthesis routes for certain compound from the unknown starting…

Q: [1] LDA [2] CH3I

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Q: How many alkene products can form from the following reaction, including rearranged products? Mark…

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Q: (a) H₂O 10% H₂SO4 OCH₂CH3 o O (e) OH H₂SO4 heat HCI major product minor product

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Q: (b) Show the mechanism of this reaction using proper arrow push notation. You mu intermediates,…

A: We will write the mechanism of the given conversion

Q: Please give the explanation of the concept and please provide detailed solution

A: Step 1: Step 2: Step 3: Step 4:

Organomagnesium compounds

The interaction of alkyl halide with Mg metal in a suitable ether solvent is the common method for the synthesis of the Grignard reagent.

Hydrolysis Grignard Reactions and Reduction

Organomagnesium halides are Grignard reagents. Francois Auguste Victor Grignard, a French chemist who received the Nobel Prize in Chemistry in 1912, created these highly useful reagents.