How would you synthesize 2,7-dimethyloctane shown below from acetylene? You must show reactions with reagents and products in their correct order. Do not give mechanisms!

Q: Show how you can carry out the following synthesis with KNOWN chemical reagents/reactions. Show your…

A: Retro synthesis : It is the way to back thinking about the starting material from which the final…

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: 4. Draw a full, detailed mechanism for the following transformations. You must account for all…

A: Product of following reaction can be made by applying appropriate reaction mechanism.

Q: CO2H SO3H Br

A: Synthesize the tri-substituted aromatic compound shown below starting from toluene. In this, we must…

Q: + NH₂ H*

A: The detailed mechanism of following reaction is.

Q: show how you could prepare 5- methyl-6-bromo-1-hexene.

A: Given is organic synthesis reaction. The given target compound is 5-methyl-6-bromo-1-hexene.

Q: Please help me with the mechanism for what is described below:  1. Draw a mechanism for the…

A: The above question we have to draw the mechanism for Wittig reaction and discuss the product…

Q: How would you synthesize the following compounds from butanenitrile using reagents from the table?…

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Q: Show reaekson and don't use hend raiting and step by step solutions

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Q: Cyclohexanone + (CH₃)₂NH and continue with catalyze by H+. Predict the product of this reaction

A: Carbonyl compound reacts with the secondary amine to form an iminium ion. The iminium ion is…

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

A: Synthesis of desired product can be reached in different ways. But, I will discuss the most…

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: lov + 애 + EtOH + MeOH → N

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

Q: Partial credit is available on this question HB:/ROOR NaOCH3 OCH3

A: Filling of reagents to complete the reaction

Q: How could you prepare 3,3-dibromohexane from reagents that contain no more than two carbons?

A: First by reacting the ethyne molecule with NaNH2 and CH3CH2I will give us the length required for…

Q: A student wanted to try to make phenoxyacetic acid using hydroxyacetic acid (HOCH2COOH) and…

A: Phenoxyacetic acid can be prepared by using hydroxyacetic acid (HOCH2COOH) and NaH. Strong base NaH…

Q: Predict the Major product(s) for the following reactions. (10 pts total) Ph Ph mechanism: Show the…

A: Here  we have to determine the major product formed in the following given reactions.

Q: Predict the products from the following reaction after a mildly acidic workup. riease show a…

A: Here, an ester undergoes reaction in presence of excess CH3Li followed by acidic workup.

Q: A teacher wants to synthesize 2,3-dichlorobutane. Propose a reaction pathway outlining the steps to…

A: We are required prepare 2,3dichloro butane from 2 butanol

Q: and from H

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Q: MgBr 1. СО2 2. H3O+ О ОН

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Q: НО, (p)

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

Q: How could you prepare a three-carbon aldehyde () from 1-butyne? (Show all reagents and…

A: Since you have posted multiple questions, we will solve first question for you. Please repost other…

Q: b)Show the mechanism for the steps of the following reaction and how they give the final product.…

A: The details solution for this reaction is provided below in attach image.

Q: b) Synthesize the target below. Alcohols of no more than 6 carbons (CH2-20, n ≤6) are your only…

A: Given is organic compound. The name of given compound is 5-nonanone.We can synthesize this compound…

Q: a) b) OH معه

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Q: propose a synthetic route to meso-2,3-dibromobutane from acetylene. show all structures and…

A: Acetylene can be converted into higher alkyne by reaction of NaNH2 and alkyl halide

Q: 5. Propose a sequence of reagents to synthesize the following from benzene. Include the structures…

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Q: The acid-catalyzed hydration of the compound below gave three products. Please provide a detailed…

A: Any molecule or ion which are electron rich species are called nucleophile for example -NH2,-OH and…

Q: g. Another possible (albeit unlikely) mechanism is shown below. What sort of acid and/or base…

A: Given is reaction mechanism.Catalyst is substance that increases rate of reaction  by lowering the…

Q: The 2-ethylhexyl group is widespread in chemical products. The core 8-carbon fragment can be easily…

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

Q: how do you synthesize 5,5-dimethyl-1, 3-cyclohexanedione from acetone and diethyl malonate?

A: Aldol condensation:When aldehydes or ketones are treated with base they form aldols, which on…

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.