n-Bu n-Bu NaOH OMs triethylamine ..OMs A heat heat

Q: a. Here are two different carbonyl bearing molecules. With the knowledge you learned so far explain…

A: Oxygen is more electronegative, therefore, it gains partial negative charge and carbonyl carbon…

Q: DBU Br DMSO, heat SN1 E1 SN2 E2 Strength of Nuc/Base Conc. Of Nu/Base Solvent Leaving group…

A: The structure of DBU (1,8-Diazabicyclo[5,4,0]undec-7-ene) is  DBU is a strong base and thus will…

Q: :C: H :CI: :CI: H. CH3 C=C H -CI: H3C-C-C-CH H3C CH3 CH3 Add curved arrows for the first step. Draw…

A: The curve arrow is given below

Q: CS reagent? Scanned with CamScanner 1-propanol with the Lucas

A: Carbocation is species in which carbon is carrying  positive charge on carbon. In carbocation,…

Q: Part A What alcohols would you oxidize to obtain the following carbonyl compounds? H;C. Draw the…

A: Alcohols on oxidation gives carbonyl compounds. Primary alcohol is oxidized to aldehyde and…

Q: sbucture of vitamin A Cre tinol), ReHnol Into write the is Converted Retinal in the body Draw the…

A: The functional group of a molecule is a key component that is responsible for providing various…

Q: pls solve this ques within 10-20 minutes in clear handwriting I'll give you multiple upvotes

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Q: c) Circle the most electrophilic carbon in the structure below and explain your choice.

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Q: Br2 но-

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Q: 2. Draw a stepwise mechanism for the following reaction. Use curved arrows to show electron flow.…

A: Deprotonation of Acetals:

Q: PQ-6. What is the rate determining step of this CH2CH3 NACN CN reaction? H3C OTs acetone H3C CH2CH3…

A: Rate determining  step is the slowest step of reaction .

Q: Time left 0:31 Name these groups from left to right: CH3 CH3 H3C CH3 CH3 CH3 Oa isopropyl, isobutyl,…

A: The 1st group is isopropyl ,2nd is isobutyl and the 3rd group ia secbutyl

Q: Draw the condensation product of undecane-3,9-dione.Need answer fast i'll rate up

A: Reaction condensation product of undecane-3,9-dione

Q: AICI3 Zn(Hg) HCI para product L Toluene Succinic anhydride SOCI2 H2SO4 NABH4 AICI3 N M heat P.

A: Series of reaction: In the series of reaction, when the reactant 'X' converted into product 'Y'…

Q: Br

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Q: Complete each multi the way. Synthesis A 1) Br2, H20 2) Nao only one stereoisomer required 1) BrMg-…

A: Soln

Q: carbonyl oygen carbonyl carbon cyclohex-2-en-1-one 2) * of atoms involved in consugared pi-systom?…

A: The following thumb rules can help in order to determine the stability of resonating structures:…

Q: Match each bolded, red carbon to the label that correctly describes its substitution. CH(CH3)3 A.…

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Q: What reagent(s) will accomplish this conversion? EtLi followed by an acid wash O EtzSiCI followed by…

A: the given reaction is 1,4-addition to the alpha beta unsaturated ketone.  where the nucleophile is…

Q: H;0"/H;O/A HO.

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Q: supply reagento e) Bra Luhuw stereochemistry) NaI Be acetone' MCPBA

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Q: `NH H*

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Q: Draw the neutral product. Select Draw Rings More Erase H CI excess NANH2

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Q: CH=CH2 H2 C. "CH3 Pd / C H' CH2CH3

A: The given reaction is hydrogenation reaction which involves addition of hydrogen to C=C double bond.…

Q: Woiteaelear mechanism for disl HO OH CH, CH2-C-CH, CH s CH,CH2-C - CH, CH eyeliccil 3-pentanol

A: Reaction mechanism of this reaction is below

Q: item 2 Draw the cycie heactal H u ones f e HO--H HO--H Dreg the aporopriat labals to their pective…

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Q: HO3S- -CH3 Br CH3

A: Detail mechanistic pathway is given below to carry out the conversion

Q: а) b) c) OEt

A: When aldehyde or ketone react with diol or alcohol it form acetal.

Q: KHS2O3 + H2O --> (?)

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Q: Analyze the reaction below, and then provide the reagents necessary to carry out the conversion. Be…

A: The answer is given below

Q: Draw a complete arrow pushing mechanism that explains the following: Br NBS hv Br

A: N-bromosuccinimide (NBS) is used as allylic brominating reagent. 3,3-dimethylcyclohexene on…

Q: Draw all products, including stereoisomers, in attached reaction.

A: The nucleophilic substitution reaction involves the removal of a group bonded to a carbon center…

Q: what is the ansle OF 0-C-O in CH3 COZH?

A: The answer is given as follows, Bond angle in O-C-O is 120 Degree  Carbon of O-C-O is  sp2…

Q: Explai all steps to Determine the Directing Effects of a Particular Substituent ?

A: The characteristic reaction shown by benzene and other associated compounds is electrophilic…

Q: Draw a curved arrow mechanism for the reaction shown. Select Draw Rings More Erase H Na H. :N C-H H.…

A: The mechanism of an organic reaction is written by the curved arrow. The curved arrow shows the…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. CN H3O*, heat Select to Draw

A: (1) The nitriles on reaction with water in acidic medium (or the hydrolysis of nitriles) give the…

Q: Which carbocation is the most stabilized? OMe OMe OMe MeO, Me Me Me Me Me &&&& CO₂Me Me Me MeO Me D…

A: Displacement of Sigma electron with pi orbital is called hyperconjugation.  In the mesomeric effect,…

Q: (a-c) (d-e) (f-g) OH ?? H₂O, H+ CI H₂O HBr OH ?? HIO4 ...H OH H H₂CRO4 O- +Na CH3Br

A: As per the bartleby guidline for answering the multiparts question, I can solve only first three…

Q: KOH, CH3CH2OH reflux Please sele Draw Michael Adduct KOH, CH3CH2OH reflux Draw Robinson Product

A: Given ; structure of reactant.

Q: what is the best mpound to make X o Give mechamism? compound OH (b) BY BY Br Nat

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Q: 1. Show the precursors a. b. CN CN

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Q: Ph Pho -Ir(CIX(PPH3)2 B-elimination -H reductive elimination insertion oxidative addition Ph₂P- H…

A: The given question is a example of insertion.

Q: What are the possible EAS products? X out any boxes that you do not use. осн Br-Br FeBr,

A: The possible EAS product can be drawn as

Q: utoneneut-al compound in each box

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

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Q: 4. Why do we have to keep Fehling's A separate with Fehling's B?

A: The question is based on the concept of qualitative analysis. We have to explain the reason for…

Q: Please help me With an in-depth explanation

A: The boiling point of the species is dependent on the intermolecular force of attraction, molecular…

Micelles and Biological Membrane

Micelles are the type of lipid molecules that organize themselves in spherical shape in aqueous solutions. The production of the micelle is a reply to the amphipathic behavior of fatty acids. It means that they consist of both hydrophobic regions and hydrophilic regions. In micelles, polar head groups (hydrophilic groups) produce an outer layer associated with water whereas nonpolar tails (hydrophobic groups) are organized in the interior.