ÇOOH a) + SOC, CH3 1) CO2 2) H30* Mg b) CH3--CI ? ElO c) CH3-CH=CH2 KMNO4 / OH

Q: H NO2 A) H2C=CHNO2 B) CH;CH-CHNO, C) + H2C-CHNO, D) + H,C-CH2

A:

Q: Draw the substitution and elimination products.

A: “Hello. Since you have posted a question with multiple sub-parts, we will solve the first three…

Q: H-N Ad, C=C H. H3C H DN H-C-CH3 ČH3 AN Pro H CH3 H,C-0-H CH3 Identity

A: Here are the complete reactions

Q: e. -CH3 Br CH3 f. Br FOCH,CH, g. „CH(CH;);

A: The hydrocarbons can form large compounds containing numerous carbon atoms along with other…

Q: Rank the water solubility of the following compounds:

A: Given compounds,

Q: 10) 2 mole 2-methyl cyclopentanone CH3 a) CH3 b) 11) e OH b) ? Na OEt CH3 c) ? & C) CH3 CH3

A: Ist question:  Answer of ist question is (a) , explained with a mechanism.

Q: a. -CH2OH b. -CH2B1 c. –CH(CH3)2 -CH3 OH- -CH,CH,Br H- -CH3 -CI -CH,CH2OH –CH¿OH -CH,CH,CH,Br

A: Priority to the atoms/group of atoms are given according to Cahn-Ingold-Prelog rules/principles.…

Q: COCI CH;NH,. b. CO2CH2CH3 1. CH;CH;MgBr 2. Hy0* с. CH;OH H2SO4 - CH3

A:

Q: h. + i. H* H3C- -0-CH2CH3 H,0 j. H* OH H3C O~H + H3C.

A: (h) Nucleophilic addition of secondary amine occurs with ketone and after that loss of water…

Q: C HoC C -CH3 2 H-Br: CH3 H3C D CH3 CH CH3 2 н- H3C E CH3 CH3 :Br -Br H3C CH

A:

Q: CH CH3 CH3 (I) „CH3 (II) „CH3 (III) CH, (IV) (V) IOH CH HO Step I

A:

Q: N₂ 1) Acetone H₂O C 2) CH (CO) NOCH, O A B. C. D E10₂C -CO,1 -CO,Et B) CO₂ NH COME CH coet

A: In this question, we will draw the structure of the major product which is formed from after the…

Q: о он 2. 2 KMNO4 + 3 H-C-CH- CH ± 2KOH +

A: Potassium permanganate is an oxidizing agent used for the oxidation of alcohols to carbonyl…

Q: Using any alkene and any other reagents, how would you prepare the following compounds?

A: Hello. Since your question has multiple sub-parts, we will solve first three sub-parts for you. If…

Q: CH3CH2=CH う CHg CH2と-H と HC三 CH लउक वररटमक cis-2.3-die thy lo xirame

A:

Q: CH3 CH3 CH C-C=CH CH3-CH,CC=CCH, CH3 IRE REI H3C H3CH2CC=CCH2CH3 H,C HCC CCH,CH3 ERI RIE Select one:…

A: Ozonolysis mechanism:

Q: CH30 ¯ Na* CH3OH A CH30 ¯ Na* CH3OH + в CI Br OH D H2SO4 A (-H2O)

A: Generally, alkyl halides on reaction with strong base undergoes elimination reaction. The product…

Q: CH3O H* CHСCH-CH(CH)2 + H,0 CH3CCH2CH(CH3)2 + ? CH3Ó

A: Ketals and acetals are formed by reaction of the carbonyl with alcohols (methanol or ethanol) in the…

Q: Ч Р 5 ____ Br I Н Cl — C — C — C —C —C = С | | CIH | | HCI Н Br HH Br H |||||||| |…

A: The IUPAC rules for naming the compounds are: 1. Select the longest chain of carbon. 2. Numbering…

Q: (g) (e) -OH-CH=CH-_1_C1₂ CH₂-C OH CH₂ CH₂ HCUN O Heat KMnO4, hot H* 1. NaBH4 2. H₂O

A:

Q: 2NaOH CO Na HCI O-O CI + O-H H20, 0-5°C C

A: First step is formation of sodium phenoxide ion.

Q: i some CH =CH2 r ? It CHz Cl

A: The IUPAC name of the given compound is : 5-Chloropent-1-en-3-ol. In this compound third carbon is…

Q: name of the #. f) CH, CH=CHCH-CH3 I. Give he IUPAC a) CHz- CA - CH CH. Br 6) CH; - CH - CH - CH, CH,…

A:

Q: 1. CHзCH2MgBr excess d. CHCHCOCHЗ 2. Нзо" HCI е. + CH3OH

A: Applying concept of organic synthesis and readent.

Q: eHschzcभे ा_ CH्- BxcH3cH, ट CH2ल,CH3 ॐ©्भु ह पर्ी 0ठितश ेब beis 2o Aheंग ecive नेब्यवुरी।

A: Here we are required to predict the mechanism of each step to convert the Starting material to…

Q: CI H,0 А (substitution) e) -CH3 H,0 B + C (elimination) major minor

A: A substitution reaction is a class of chemical reactions in which an atom, ion, or group of atoms…

Q: нонн онно С. Н.N-C-с-N-C-с-N—с-с-он CH;CH¿CHCH3 CH3 C,H;CH2 нонн онно T |LI I |LI I ||…

A: Q. C In the peptide chain, the 1st amino acid is isoleucine 2nd amino acid is alanine 3rd one is…

Q: u OH OH CH₂ CH₂ ‡ Br -CH₂ OH unrelated R He OH strudel isquer H₂Cy Br OH Br CH₂ 3 R

A: R/S system of nomenclature : It is a naming system used for assigning absolute configuration to…

Q: H3C. CH-CH2CH2 Br H3C NANH, / NH3() CH3CH2-CEC-H

A: In organic reactions, a nucleophile attacks an electrophile.

Q: 1. 2 3 CH, -C =e CH2- CH = 3. 2. er-1- - 4 - আইন 3. CHO

A: Given compounds are :  a).  b).  What is the IUPAC names of the following = ?

Q: Draw the products of the following reactions

A: Given reactions,

Q: LIAIH, d. CoHs-C-CHз H+ е. CоHs-C-СH NaBH, H+ f. C6H5-C-CH3 Br2 NaOH

A:

Q: H. CH3 H H H CI H. CH, H H C-C C C C C H H C- C-C C-C H- H H H H. H H H H 3-methyl hexane…

A: Stereoisomers which are non-superimposable mirror image of each other and rotates the plane of plane…

Q: -С-NCH-CH3 + HCI H2O H-0 a. ČH,CH3 1. CH3CH2MgBr 2. Нзо* b. CH;CH,ĊCH3 с. + (C,Hs)3P=CHCH3

A: Note: According to our guidelines we are supposed to answer only first three subpart.

Q: H-CEC-H

A: Organic synthesis is a process of making organic molecules in a convenient pathway.

Q: k. H2C=CH- -C- CH3 NABH4

A: The given reaction is reduction reaction in which carbonyl group will convert into alchols.

Q: LIAIH4 (©) CH;CH;CH;I CH;CH,CH3 + - (d) H Ph H Ph C=C H;C-C-C-H H;C ОН ОН

A: Alkenes are compounds containing a double bond between carbon and carbon. The general molecular…

Q: H-a Oi - :ö: + :CEN CN CH;-CH=CH, H-a CH3-ČH- CH2

A:

Q: 1. 2. CH-CI 12- - --> OH XI OCH3

A: " Since you have posted a question with multiple sub-parts, we will solve first three sub-parts for…

Q: HC-C C-CH, Undlar catalyst Oa Ceton b. Alqueno cis C Alcano 0a Adehdo Alqueno trans

A: The  name of  given reactant is  2-butyne which is  an alkyne.

Q: SCH4U1-YA Orgo Quiz a. H;C-CH; CH3 CH;–CH;-ĊH–CH–Hċ–CH, CH3 CH CH3 b. H;C-C=C-CH,…

A: The IUPAC names of the given compounds are.

Q: CH3 CH2CH3 CH;CH, CH3 - C- -CH2- C- -H- CH3 Cl CH H Н н H3C H;C -C-C C-H

A:

Q: g. H;C NH, h. i. H* H;C-C~o-CH2CH3 H,0

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: Identify the catalyst in each equation.

A:

Q: (a) CH3 (b) он (c) OH CH3CHCHCH2CH3 ČH,CH2CH3 HOCH2CH2ĊHCH2OH H. но (d) он (e) Ph. он (f) OH H CH3…

A: Note - Since you have posted a question with multiple sub-parts, we will solve the first three…

Q: CH3 H. H CH3 H H;C- H. CH3 (а) II or mationcohexane has a ter e H. CH,CH,CH3 H. CH,CH,CH3 H. (b) II…

A:

Q: H. (a) + D-CI + H-CI H. H. H. OH (b) +H-CI e CH CH,

A:

Carbohydrates

Carbohydrates are the organic compounds that are obtained in foods and living matters in the shape of sugars, cellulose, and starch. The general formula of carbohydrates is Cn(H2O)2. The ratio of H and O present in carbohydrates is identical to water.

Starch

Starch is a polysaccharide carbohydrate that belongs to the category of polysaccharide carbohydrates.

Mutarotation

The rotation of a particular structure of the chiral compound because of the epimerization is called mutarotation. It is the repercussion of the ring chain tautomerism. In terms of glucose, this can be defined as the modification in the equilibrium of the α- and β- glucose anomers upon its dissolution in the solvent water. This process is usually seen in the chemistry of carbohydrates.

L Sugar

A chemical compound that is represented with a molecular formula C6H12O6 is called L-(-) sugar. At the carbon’s 5th position, the hydroxyl group is placed to the compound’s left and therefore the sugar is represented as L(-)-sugar. It is capable of rotating the polarized light’s plane in the direction anticlockwise. L isomers are one of the 2 isomers formed by the configurational stereochemistry of the carbohydrates.