Draw structure(s) for the product(s) that you would predict in the following reactions. Show reasonable mechanisms for the processes in the boxes provided below each reaction.

Q: dilute HCI

A: The addition of HCl to alkene yield alkyl chloride. The addition process follow Markovnikov rule.…

Q: 4. Provide the full mechanism (curved arrows and intermediates) that leads to the product in the…

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Q: Identify reagents that can be used to achieve the following transformation: OH The transformation…

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Q: Complete the synthesis of the following compound from the starting material given (2-…

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: |Propose a full and reasonable mechanism for the formation of the unusual MAJOR product shown in the…

A: Carbonation: Carbocation rearrangements can be defined by the movement of the carbocation from an…

Q: Complete the synthesis of ethyl (E)-2,2,4-trimethyl-3-oxo-5-phenylpent-4-enoate from the starting…

A: Ester molecules can undergo substitution or nucleophilic addition reactions. The alpha hydrogen,…

Q: 2. Propose multi step synthetic routes from 1-butanol and the given organic molecule to the…

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: Starting with benzene and using any other necessary reagents cases, there may be more than one…

A: Given is organic reaction. We can prepare given target compound from benzene by using various types…

Q: 6) Show the two most stable products (no mechanisms) that can be formed when the following compound…

A: Step 1: Step 2: Step 3: Step 4:

Q: Propose a synthesis for (Z)-hex-2-ene; you may use any reagents that you wish, so long as they add…

A: We have to synthesized (Z)-hex-2-ene.

Q: Propose a reasonable mechanism using curved arrows for the following transformation. You should…

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Q: Propose an efficient synthesis for the following transformation. Use the reagents/conditions below…

A: In first step alcohols react with reagent 4-Toluenesulfonyl chloride in pyridine solution to yield…

Q: Propose an efficient synthesis for the following transformation: لا تمليلة The transformation above…

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Q: ive the complete mechanism for the reaction below. The major product should be that of something…

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Q: Using curved arrows to indicate electron movement, propose a mechanism for the following…

A: Benzene mechanism (elimination- addition)

Q: Starting with benzene and using any other necessary reagents of your choice, design a synthesis the…

A: Benzene is first acylated using reagent B. Then it is reduced using reagent E. Nitration is done…

Q: (c) Hint C4 => C5! ОН Н =0

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: 2. Propose a set of reactions that will convert cyclohexanane into target molecules A and B. You are…

A: Here substrate is alpha beta unsaturated carbonyl compound.  For the formation of TM A , we have to…

Q: give the product (s) of the reaction when it reacts with HBr/ROOR in presence of heat or energy.…

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Q: 2. Show how you would synthesize the molecule shown below by starting with ethyne and any other…

A: With the addition of water, alkynes can be hydrated to form enols that spontaneously tautomerize to…

Q: Propose a synthesis and give detailed comments on each reagent you used and why you wouldn't use…

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Q: lov + 애 + EtOH + MeOH → N

A: The question is based on the concept of organic synthesis.  we need to synthesize the product using…

Q: O [H]

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Q: Propose an efficient synthesis for the following transformation. x-1 The transformation above can be…

A: The question is based on the concept of organic synthesis.  we need to synthesize the product using…

Q: Propose an efficient synthesis for the following transformation: The transformation above can be…

A: The concept used here is from organic chemistry.  According to question.  Here LiAlH4  will reduce…

Q: Propose an efficient synthesis for the given transformation. OH This transformation can be performed…

A: First epoxide is formed from given alkene using mcBPA ie. H and then epoxide is opened by attack of…

Q: Propose an efficient synthesis for the following transformation. X سر A The transformation above can…

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Q: a) Stereoselectively b)

A: Note- Dear student, since the given question is a multiple question, hence I solved first question…

Q: When the compound below is treated with catalytic sulfuric acid, an equilibrium mixture of many…

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Q: (b) HDAB The transformation above can be performed with some reagent or combination of the reagents…

A: Given that, a reaction scheme is shown below We have to carry out the above transformation.…

Q: Suggest how you would carry out each of these syntheses

A: The given compounds can be synthesized as follows: 1)

Q: 1a) Provide the mechanism of the reaction below, catalyzed by triethylamine. The reaction should…

A: The given reaction is a type of nucleophilic addition reaction followed by an elimination…

Q: Please show the products of following reactions and reaction mechanisms for each using the right…

A: Potassium t'Butoxide is a bulkier stronger base and poor Nucleophile so that it will give major…

Q: 5.) Provide a mechanism for the following transformation using proper arrow pushing rules. While you…

A: This question belong to reaction mechanism of organic compounds that is Electrophilic Aromatic…

Q: CH H;SO, HO- CH

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Q: Propose a synthesis for each of the compounds below from benzene. It will take 4 or 5 steps, be sure…

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Q: : ☐ + T ☑ Add the necessary reaction conditions above or below the arrow in this organic reaction.…

A: The required answer is given below Explanation:Step 1: Step 2: Step 3: Step 4:

Q: D phng Br, EtzO_ Locty OCH3 2) Hz0

A: The answer is given below

Q: Provide the synthesis, including the substrate, major intermediate(s), reagent(s), and product for…

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Q: Propose a plausible mechanism for the following transformation. For the mechanism, draw the curved…

A: Here in this question we need to find out the mechanism by which the given conversion will take…

Q: Show how you could prepare the following alkyne in a multistep synthesis starting from…

A: The reaction of 1-bromo-3-methylbutane to form the given alkyne involves a chain of multiple…

Q: Propose an efficient synthesis for the following transformation. مدل The transformation above can be…

A: The question is based on the concept of organic synthesis.  we need to synthesize the product using…

Q: Icorrect. Propose an efficient synthesis for the following transformation: The transformation above…

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Q: Br Br **||||| е OMe MeOH, RT of t-BuOH, RT S PrSH, 40°C

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

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.