III. NNCH3 MeOH OCH 3 OH OCH3 б IV. 0= OH MeOH

Q: Write the chemical equation involved for a specific EAS reaction,-Electrophilic Aromatic…

A: We know, EAS means Electrophilic Aromatic Substitution. Electrophilic substitution involving…

Q: the question is asking to: "provide a synthesis for the following reaction. if more than one step is…

A: The reaction taking place is given as,

Q: Click the "draw structure" button to launch the drawing utility. What product is formed when the…

A: K2Cr2O7 is names as potassium dichromate. It behaves likes and oxidising agent. It will oxidise…

Q: Question attached

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Q: be + NaOH ?

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Q: (a) HE H -H H₂N² Give TUPAC Name (b) Corive mechanism with Curved arrowsg th-el-

A: According to IUPAC nomenclature  an organic compound is named by identifying molecule's longest…

Q: For each of the following molecule circle the one that is more stable. Jus your answer by marking an…

A: Note: Since you have posted a question with multiple sub parts, we will provide the solution only to…

Q: Please redue or give back the question Because I asked for the structures to be drawn out!

A: It is a follow up question.

Q: Alkanes can undergo all of the following reactions except for Opolymerization O halogenation…

A: In this question we need to Identify the reaction ftom the given options which is not possible for…

Q: Please fill in the blank for both sentences.   Infrared radiation is to IR spectroscopy as…

A: NMR and IR are the useful technique for structure interpretation .

Q: Draw the structure(s) of the major organic product(s) of the following reaction. CrO3/H3O+

A: CrO3/H3O+ oxidizes primary alcohol to carboxylic acid and secondary alcohol to ketone.

Q: 2) For two of the following pairs of compounds, identify the most basic atom in each compound, and…

A: Here we have to find the most basic atom and the most basic compound from the given pair of…

Q: draw a triol compound containing a LABELED primary, secondary, and tertiary alcohol.

A: Primary alcohol :- The compound in which a  carbon atom which is connected with only one alkyl…

Q: If the elimination reaction can result in the formation of two different alkenes which one with…

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Q: Hofmann Elimination Reaction NH₂ Draw all missing reactants and/or products in the appropriate boxes…

A: Hoffmann elimination rule :

Q: Draw the structure for cis-1, 3- dibromocyclohexane (with the ring) And the structure of trans-1,3-…

A: The objective is to draw the structure of the given compound. The cis and trans forms describe the…

Q: Give a clear handwritten answer with explanation..given below a energy diagram...what represent A in…

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Q: f OH

A: A pair of substances which are non-super imposable mirror images are called enantiomers.A pair of…

Q: Provide the correct IUPAC name for the skeletal (line-bond) structure shown here.

A: The correct IUPAC name of the given skeletal structure given below.

Q: Draw the Conjugate Acid of the structure with it's lone pairs.

A: Step 1:Step 2:

Q: Draw the curved arrows that accomplish each of the following transformations. H by- 4- 10 O-H

A: we have to draw the curved arrow to accomplish given transformation.

Q: NBS hv

A: NBS gives allylic bromination.

Q: e) why are they organic products in the reactions from (chemical equation for acid base reaction of…

A: Solubility of a compound is largely dependent on the solvent.

Q: How many monochloro substitution products are produced when the alkane below is chlorinated?…

A: The given structure of the alkane is . We have to tell the number of different monochloro…

Q: a) electrophilic aromatic addition reaction C) nucleophilic aromatic addition reaction nucleophilic…

A: The question asks about the category under which the nitration reaction of benzene with HNO3 and…

Q: Check the box under each structure in the table that is an enantiomer of the molecule shown below.…

A: Opt out the enantiomer of the given organic molecule.

Q: Convert the following skeletal drawing into a wedge and dash drawing. Be sure to show all H in the…

A: In a wedge-dash representation, the stereochemistry of an sp3 hybridized carbon is shown.

Q: answer with explanation..complete the reactions with detailed given below

A: In this question, we will write the all the synthesis steps for the given transformation by using…

Q: Name the alkenes below. a) b)

A: In first step, we identify functional group present.We make longest carbon chain possible.While…

Q: Be sure to answer all parts. Draw the products of the reaction of cyclopentanone hydrazone heated in…

A: When cyclopentanone hydrazone is heated in presence of triethylene glycol with sodium hydroxide ,…

Q: Is the attached compound an aromatic? if the compound that not aromatic, state why this is so.

A: Aromatic compounds have the delocalization of pi electrons on a planar and cyclic ring. Aromatic…

Q: from and alcohol of two carbon or less Cl

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Q: CH₂OH H

A: Here we have explain major product formed in the following given reaction.

Q: Number of x electrons in A: I Enter numeric value Compound A is: O antiaromatic O aromatic…

A: Aromatic compounds are cyclic and have alternating double bonds/conjugateed double bonds.Any given…

Q: Appropriately circle and correctly label both groups, the acetal and the hemiacetal. OH

A: We have given the organic compound and we have to circle the acetal and hemiacetal group.

Q: Give a clear handwritten answer with explanation....give the all stereoisomers with explanation…

A: Total stereoisomer depends upon the total number of chiral  center present in the compounds.

Q: Why is diethylamine more basic that methylation? ( provide structures)

A: Basicity of an organic amine compound is determined by the availability of lone pair electrons on…

Q: Weak base can react with strong acid to form a salt. If pyridine reacts with a strong acid to form…

A: Aromatic compounds are conjugated, planner and have ( 4n + 2) delocalizable  electrons.

Q: Please help what are special rules or laws to predict predominant products for alcohols or et

A: Here's a chart summarizing some special rules or laws to predict predominant products for alcohols…