HO cs Scanned with CamScamner

Q: redict the product for each of the following reactions. Be sure to show stereochemit ppropriate. Be…

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Q: Draw the products (including stereochemistry) for attached reaction.

A: Please find below the reaction along with the stereochemistry. Since the attack is possible from…

Q: Draw all products, including stereoisomers, in the following reaction.

A: The given reactant is a 3° (tertiary) alkyl halide.

Q: Draw the complete arrow pushing mechanism for the base-catalyzed keto/en the following compound.…

A: The chemical equilibrium between ketonic and aldehydic form of same substance which get formed due…

Q: n each case below select the synthetic procedure that could be used to carry out the transformation…

A: The product of the following reaction method are shown as follow.

Q: Where should Cl go in this reaction (assume major product) and why? HCI (A) Carbon (b) because of…

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Q: Draw a stepwise, detailed mechanism for the dienone–phenol rearrangement, a reaction that forms…

A: Please find below the reaction mechanism.

Q: AlCl3 + Cl,

A: Given :-Here , we have to complete and frawthe stepwise mechanism.

Q: Draw the product formed from the ring-closing metathesis of eachcompound. Then, devise a synthesis…

A: 1- First we will see tha Products for each by using ring closing metathesis.

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: :ÇI: CH3 + KOTBU H,C ČH3

A: Here, strong base/nucleophile is present, so there is a possibility of substitution as well as…

Q: Alkyl substituents are: Select one: O a. Strong, meta directors O b. Strong, ortho/para directors…

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Q: Predict the stereochemistry For the E2 reaction Draw a Newmann Projection Of the reactive con…

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Q: Draw the mechanism ffrom benzaldehyde to this using:   i)NaBH4 ii)TsCl, py iii)NaCN iiii)H+,…

A: Given,  The mechanism for target product formed from benzaldehyde by using  i)NaBH4 ii)TsCl, py…

Q: Draw the product of attached reaction

A: Organometallic reagents are very useful in the field of chemistry as they can make a variety of…

Q: Draw all possible constitutional isomers formed by dehydrohalogenationof attached alkyl halide.

A: Number of functional group is associated with organic compounds which impart specific chemical and…

Q: ÇI NaSCH3 ? Be *very specific* about the stereochemistry of the product(s) of this reaction 18.

A: Given: Observing the given alkyl halide shows that it is a secondary alkyl halide with a good…

Q: What reagentls) will perform the following miction?

A: The given reagent is a ketone. It belongs to the carbonyl family. the IUPAC name of the compound is…

Q: Please draw the possible resonance structures for the following carbocations.  Please demonstrate…

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Q: Draw the keto tautomer of attached enol.

A: Two molecules that have a similar molecular formula but differ in the way how their atoms are…

Q: 1. Complete the reaction mechanism (Please draw all of them) -Ql Carbanion Enolate Dibenzylacetone…

A: The carbon atom double bonded to oxygen atom and single bonded to two alkyl groups is called…

Q: prese Maxwell Draw the major organic product of the reaction shown. Select Draw Rings More HI H3C-OH

A: in nucleophilic substitution reaction nucleophile attacks on substrate and forms product.

Q: For Mhis reaction, draw the majar organic products and show the important stereochemical Of the…

A: Consider nucleophilic substitution reaction with stereochemistry of reactant and nature molecule.

Q: alkene that, upon ozonolysis reaction, gives only H. H' Select one:

A: In this question we will Identify the starting material Alkene which give di-aldehyde Product.  You…

Q: reagents you deem necessary. Be sure vour synthesis vields the correct stereochemistry

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Q: Synthesis F Please Include the reagent and intermediate as well as the Meta direction OH acyclic…

A: The desired product can be made by using Diels-Alder reaction. The detailed mechanism is in the next…

Q: Provide a synthetic route to the following compound(s) а. Br он from "H b. from SCH3

A: a) Since the configuration of carbon is changing in the product. Hence it means the conversion of…

Q: (d)Predict the stereochemistry of the final product with proper explanation. Me ??? Me Me THF (+)

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Q: Draw the major organic product of the reaction. Ignore stereochemistry

A: First step is the formation of stable carbocation.

Q: Draw an alkyl bromide with proper stereochemistry that can be used to synthesize the given alkene as…

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Q: rovide all reagents and solvents as well as additional organic substrate necessary to perform the…

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Q: O.

A: The isomers have the same molecular formula but a different structural formula. In the keto-enol…

Q: O2N. Br

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Q: HO OCH3 OCH3

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Q: Provide the whole reaction mechanisum teneration of electrophile, nudeophile bond formation, bond…

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Q: Keto-enol tautomerization occurs rapidly and favors the formation of the enol product. Select one:…

A: The reactive methylene compounds exhibit keto-enol tautomerism where the H-atom of the methylene…

Q: A)

A: Here we have to prepare the following given compounds from alkyl halide containing four carbon atom…

Q: CI NH pyr

A: Answer

Q: Draw the product (Y) of the following reaction. Show how the transition state determines the regio-…

A: This is an example of Diels-Alder reaction

Q: Identify the suitable reagents for the following: ol or Br2 MINOA MADR

A: Addition of Br2/H2S to an alkene.

Q: Which of the following alkene addition reactions occur/s specifically in syn fashion?…

A: If we say a reactions occur/s specifically in syn fashion, the adding atoms should be on same side.…

Q: (d) Explain the observed stereo-selectivity in the formation of product using Chelation model. OMe…

A: The mechanism of this reaction is done in the below.

Q: Draw the major organic product for the reaction shown. NH LIAIHA

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Q: how an alkene be coverted into carbonyl compound in one step?

A: Ozonolysis: The unsaturated bonds (double, triple or azo compounds) are cleaved with reductive…

Q: Addition of water to an alkyne gives a keto-enol tautomer product. Draw the ketone that is in…

A: alkyne addition with water to give enol form  Enol participate keto enol tautomrism Ene =double bond…

Q: Give the mechanism given bleow reactions with curved arrow and all format harges ? 1-ct y

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Q: Draw the major product(s) for reaction of methyl pentanoate with: LIAIH4; then H30*

A: Ester on reduction with strong reducing agent LiAlH4 followed by acidification gives primary…

Q: An alternative solvent to alkylate saccharin nucleophile could have been another OA. protic; ethanol…

A: Given statement is :  An alternative solvent to alkylated saccharin nucleophile could have been…

Q: Draw the equilibrium chair confirmation of cis1-chloro-3-methylcyclohexane. Interpret the E2…

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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.