PCk H,-Pd BaSO4 CH;NO, 1,0 CH;O OCOC- CH;0 CO,H СНО NAOH (Rosenmund reduction) OCH3 OCH3 OCH3 OCH3 OCH, Na-Hg CH;O CH-CHN Ο, CH;O CH,CH,NH,

Q: please explain the reaction with mechanism

A: in the given question, it is secondary alkyl halide which reacts with a very good nucleophile. This…

Q: NH₂

A:

Q: OCH3 OCH, CH,N2 NH,, in aqueous CH;0 COCI CH;O СОCHN2 AGNO3 OCH3 OCH3 diazoketone OCH; OCH3 LIAIH4.…

A: The detail solution is given below

Q: b) ОН CH3 ОН

A: Elimination of alcohol gives alkeneHydroboration oxidation of alkene gives anti-Markovnikoff…

Q: Draw the final organic product for this reaction: NaOH

A:

Q: mechanism, please explain each step because I need understand

A: Ans. Isomerization and hydroisomerization of normal paraffins to conversion in monobranched and…

Q: Propese the below epoxide Starting with cycloheptanone a mechanism for HC CH3 SCH3 CH3 CHs

A: Detail mechanistic pathway is given below

Q: Indicate the preferred/major product for the following reaction. Assume a proper work-up. Ci C2H5…

A: We have to give ans with explanation and mechanism  as follows in step 2:

Q: Please show and explain mechanism

A: We have to predict the mechanism for given reaction.

Q: Draw the product of the following reaction, indicating the correct stereochemistry. Ili CH,OH H,SO,…

A:

Q: Give reaction of glycol and  ketone with mechanism. Detail explanation

A: Glycol is used as protecting  Group  for ketone and aldehyde

Q: complete the reaction, show detailed mechanism

A:

Q: Please give mechanism with name of all of compounds and product and all other steps

A: NaBH4 is mild reducing agent, as it is insoluble in non polar solvents, therefore alcoholic or…

Q: Provide the major organic product of the reaction shown below. 1) Н2О, Н.О. А 2) CH CH OH, H.Oº, А…

A: -> In presence of H2O /heat and acidic medium Acetal can break and form carbonyl compound. ->…

Q: NaOH, H20 Cl CH2OH ÇO,H ÇO,H ÇO.H C) D) B) A) Cl HO, Cl CH2ONA ČH2OH CH,OH ČO,H

A: ->NaOH is base hence, it can abstract most acidic hydrogen present in the given compound.

Q: i 1. PhNH2 2. KCN 3. H₂O *H₂N COO

A: In this question, we will use NH3 ammonia instead of PhNH2 because NH3 will give you an amino acid…

Q: X retinal (vitamin A aldehyde) important for vision + NaBHA 2. H₂804 Zad

A:

Q: (a) PHOOC-CH,-C-CH,-COOP. (1) KCN, A (2) H,0® (o) СООН Onl

A:

Q: Draw the final organic product for this reaction:

A: Here first of all , the base (NaOH) abstracts the proton from the diketone to produce an  enolate…

Q: цо что TMS CI OTMS сизмде Изо+ НО 0TMS F- Иго э цо он a

A:

Q: Give me mechanism. Please explain each step!

A: Following is the polymerization reaction of the given alkene.

Q: i. H,C CH3 CH, c-CH CH CH CH H,C CH3 Он Br ii. HO HBr

A: Organic synthesis examples.

Q: Draw a reasonable mechanism for the following reaction: H heat H-CEC-CH3 Br2 H-CEC-CH,Br C=C=C Br

A:

Q: CH(COOK)2 (3) CH(COOK), Electrolysis (b) odiyidtam-S

A: this is the mechanism

Q: Br2, aq. NaOH NH2

A: Hoffmann bromamide reaction is a reaction where primary amines are prepared. The amine obtained will…

Q: 51. What is the main product of the following reaction? 1. Br2, NaOH HO D. Br Br 2. H3O* А. Br В. С.

A: Bromoform reaction.

Q: what will he major mdult of the following reackione 9gmine inngamat.byproduete I.03 2 zn, HOAC

A: It is one of the crucial reaction of alkene where carbonyls are major outcomes.

Q: (ii) CO₂Me 1) Zn/Cu, CH₂l2 2) Et₂0/reflux

A:

Q: Br Ph-Li Br

A: Reaction of 1,1-dihalocyclopropane  with Ph-Li yields the majour product allene. Reaction: When…

Q: 1. 1 equivalent LDA 2. Br

A:

Q: N OH N NO₂ 11 (not isolated) 1% Pd/C (2 mol % Pd) H₂ balloon, HCI (3 equiv) 2 wt% TPGS-750-M/H₂O 75…

A:

Q: Br (CH3)COK + CHB13 Br (CH3);COH

A: Singlet- Carbene :   This Carbene  has a lone pair of electron for donation again , it has a vacant…

Q: NH₂ OH 4-aminophenol + CHO Acetic Acid PC12CHO EtOH OC12H25 4-(dodecyloxy)benzaldehyde C12H25O HC OH…

A:

Q: H2N CH,COCH,Br S-ル

A:

Q: n-Paraffin acidic cata iso. Poraf fin ^ H AICI3

A: Isomerization of is the process where a compound is converted into one of its isomeric forms. That…

Q: -Br но-

A:

Stereochemistry and Isomerism

Stereochemistry deals with the three-dimensional structure and properties of molecules. It explains the arrangement of atoms and their manipulation within a molecule in a 3D structure. Stereochemistry can be dealt with all types of molecules. Based on the stereochemistry of a molecule, the physical and chemical properties of the molecules vary.