Q: He CH3 H3C- HO- OH CH3 OH H. CH3 H. HO.
A:
Q: Name the 3. CH=CCH,CH=CH, 10 er CH, 4. CH,CCH,C=CH CH, 5. CH,CH,CCH,CH, CH,
A: Naming of alkenes and alkynes is done by first identifying the longest chain of carbon atoms that…
Q: HC= CH H3C-C-OH CHCH (CH),CHCH;C=CH (CH),CHCH, он CH;CH,C=C-H CH;CH,CHCH,CH,CH3
A: In this question, we have to find out the correct answer of given problem by the help of the…
Q: Into how many peaks will each proton shown in red be split?
A: a.
Q: H,N CH2CH3 CH,CH,NH2 b)
A: Nomenclature: With he help of iupac nomenclature we are enable to study the organic structure…
Q: What would be the condensed formula for the structure?
A: Condense formula of any molecules or chemical compound is a representation of the given formula…
Q: CH,CH,OH CH, `CH3 H* CH3 но
A:
Q: + Hz Ni > !! L:AI Hy, Ether CH3 C -OH Hao ○こ
A: 1. The reaction of cyclopentanone with H2 in the presence of Ni-catalyst leads to the reduction and…
Q: NH-C-CH3 CHa CH, O
A: The question is based on the concept of organic reactions. we have to convert the reactant to…
Q: Give the IUPAC name for each thiol.
A: IUPAC names : (a) Pentan-3-thiol (b) Cyclohexanethiol (c) 5-ethylheptan-1-thiol
Q: CH3OH он Rxn 1 CH,OH Br LOH Rxn 2
A:
Q: HO- CH2CHCH,-OH |CH;CHCH,–OH CH,CH2CH2 –OH CH,CH2OCH3 OH OH
A: surface tension depends on intermolecular force of attraction between compound. as the…
Q: d. (d) CH;CH2CH2CH,CH(OH)OCH3 е. (е) CH;CH,CH,CH,CH(OCH3)2 f. (f) HO,
A: Tollen's test is used to distinguish aldehyde functional group from the other functional groups in…
Q: CH3CH=CHCH,CcOOH ----> CH3COH + HOCCH2COOH
A:
Q: What is each compound’s systematic name?
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Q: 1. CH,CH; CI AICI, HANNH2. ОН, Д 2. H:о CH:CH:CH, CH:CH;CH:OH a. d. CH CH: CH, CH CH а. е. он CH CH,…
A:
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: O C5 H12 CH3-NH, ⒸHO-CH₂-CH(CH3)-OH O C₂H3 CN
A: Answer - The correct option is (c) HO-CH2-CH(CH3)-OH Explanation - According to the question -…
Q: NH2 CH3 b. CH,-CH-CH-CH-CH, N-H d. С. -NHCH3 а. CH3 e. CH-N-CH-CH, NH3 CH;-CHCH, + OH
A:
Q: H20, H2SO, (h) H&SO, (i) CH3-C=c-CH3 + H2 Lindlar CH3OH B H2SO, Br2 (6) CH,-CH=CH-CH, 2NANH, B
A: Since you have posted a question with multiple sub-parts, we will solve first three sub-parts for…
Q: NaNH, CH;CH2-Br OH NaNH CH CH,a b) CH,CH,C=CH NH C-H HCl . HCl CH;OH CH3OH
A: "Since there are multiple subparts, we will answer only the first three subparts. If you require the…
Q: CH- CH OH -> )CHy-CHCH-CH2 CH-CH-CH d) Cig-CーCH-CHy OH OH e) CH ーぎ
A: Oxidation is the addition of oxygen to a molecule or the removal of hydrogen from the molecule.…
Q: (g) NH + CH3(CH2)6CH,CI ethanol (h) -CH2CI + NH3 ethanol
A:
Q: Name the following:
A: Since the question has multiple sub-parts, we are entitled to answer only the first 3 parts.
Q: OH CH-CH2 CH CH CH3 CH, CH,
A: The IUPAC name of a molecule includes its chemical structure as well as sterochemical configuration.…
Q: OH CH,CHCH,CC=CH CH, CH3 Çi C1 CH 3-CH-CH 2-CH-C-CH-CH 2-CH2-OH tH-CH, C1 CH3-CH,-CH;-CH2-NH,
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Q: E) NaoH CH docHs CH3 CHz CH3 KOH F) ¿ CH Ćo CH3 CH,) CH
A:
Q: a) CH;SH + H2O CH;S + H,O* b) CH;CH,NH2 + H2O → CH;CH,NH, + OH
A: In 1st reaction H2O behaves as base and takes acidic hydrogen from CH3SH.
Q: How could the following compounds be synthesized from acetylene?
A: Since you have posted multiple sub-parts, we are entitled to answer only first three.
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
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A: Given compounds,
Q: C-Cl + NH, - a. || N-CH,+ CH,C-OH- b. | CH, || c. CH,CH,- N-CH, + CH;-C-Cl→ CH, d. N-H+HCl- N-H+ H,O…
A:
Q: H,C- -CH- -CH3 1 CH3 2 H;C- CH-CH ČH,-CH; H,C-CH,-CH,-ÇH-CH;-CH;-CH; 3 ČH;-CH3
A: “Since you have posted a question with multiple sub-parts, we will solve first three sub-parts for…
Q: H,C-CH,-ö-CH, + :Br: H,C - C - Br : CH,
A:
Q: Draw the products of the following reaction:
A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…
Q: ) CH, CH C H2 CH CH3 CHz OH 2) CH, CEC CH CH, CH, OH CH, CH= CH CH, CH CH, OH 3)
A:
Q: Fill in the boxes
A: The reagents and the products are :
Q: CH;CH2CH2CH»ĊCI CH3 CH;CH,CH;COCH,CHCH, CH3CH,CH,CH,CH;CN(CH3)2
A:
Q: CH3 Brz/H,O A) CH3 CH3 1) BH/THF B) 2) H-О, NaOH CH3 CH3 CH3COOH C) CH3
A: Reaction is called bromination of alkenes. Solvent used is water. In this reaction solvent is very…
Q: What is the major product obtained when each of the following alcohols is heated in the presence of…
A: The reaction of alcohols with sulphuric acid, elimination of water molecules can occur. This is…
Q: CH3 H3C CH3 CH3 CH3 H- -OH H2N- g. h. H3C Br H Br i. NH2
A:
Q: HBr А. OH CH3 CH3 H-C-Č- -CH3 OH H ÓCH,CH, OCH CH CH3 [1] CH,CH,O Na* Br OH HO. Br [2] H20 OH…
A: In the acidic medium carbocation is formed and SN1 reaction happens. In the basic medium SN2…
Q: Draw the keto tautomer for each of the following:
A: The given molecules are represented as follows:
Q: Give the complete IUPAC name for each of the following compounds:
A: IUPAC name of (a) Butan-2-ol IUPAC name of (b) 2-iodo-3,3-dimethylpentan-2-ol IUPAC name of (c)…
Q: CH3 CHzCH CI OH-
A: Answer
Q: CH3 CICH,ÖCH,CH,CH(CH,), CH,CH,Č-CHCH, CH, Č,H, ČH2CI CH3 OH .CHO `CHO оно BRCH,CH CCH, CH,CH,CH,CHO
A: Given molecules are : Provide the IUPAC names for the following compounds = ?
Q: Which is the stronger acid?
A: Acid is a compound that donates proton and base is a compound that accepts a proton. The strength of…
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- 5. Consider the following pairs of structures. Identify the relationship between them (enantiomers, diastereomers, or identical compounds. он HO o CH,OH H,C H но CH,OH сон H HO. HO CH, HO,C CH COH HO,C, CO,H CO,H н онн он н онн он HOH,C сно OHC CH,OH Br CH,CH, H,CH,C CI CH OH2 Identify the following pairs of compounds as identical or isomers. If they are isomers, are they constitutional isomers or stereoisomers? If they are stereoisomers, are they enantiomers or diastereomers? Clearly write the words- identical, enantiomers, diastereomers, constitutional isomers. H3C CH3 and H3C. H3C Br H.Q2 Give the stereochemical relationships between each pair of structures. Examples are same compound, structural isomers, enantiomers, diastereomers fa CH. OH HO- OR HO CH, CH. CH,
- 5. Consider the following pairs of structures. Identify the relationship between them (enantiomers, diastereomers, or identical compounds. HOH2C H OH H OH HO H Br H3C Н H H₂CH₂C CI Br H CHO CH3 I CH3 OH OHC Н H OH H OH Bell!! H3C, HO H Н.С H CH₂CH3 CH3 CI HỌ,H CH₂OH BrPart D. Do the two structures A and B of each pair drawn below represent the same molecule, constitutional isomers, or stereoisomers? If A and B are stereoisomers, further classify them as enantiomers or diastereomers. H3C Structure A H3C HO H3C H3C Br T H H3C H HO H3CC H C Br HC H H H H CH₂Br CH₂CH3 H CH₂CH3 CH₂OH OH H HO G G H HO H HO G CH3 CH3 CH3 Br Hallo H H3C H Structure B H3C CH3 Br WING H Br HOCH₂ CH3 CH3 HO H CH₂OH H CH₂CH3 H CH₂CH3 H H H H H H Gim CH3 H OH "H ·GII. CH3 HO. OH OH CH3 CH3 OH Relationship of A and BHN- H3C HN -NH "CH3 OH H. CH3 H,C. Br H3C CH3 CH3 HO. Br HO,
- Describe the stereochemical relationship between the two structures below. H H CHO OH OH CH₂OH I OA Mesomers HO H B. Enantiomers OC. Conformers D. Raceomers E.Diasteromers CHO -H -OH CH₂OH IIDraw all possible stereoisomers for HC=OCHClCHClCH2Br. Label the compounds as Compound I, II, etc.. Determine the relation of each of these compounds to another (pair relations as enantiomers, diastereomer, mesocompound or no relations).5. Appropriately label the given molecule pairs as enantiomers, diastereomers, constitutional isomers, or not isomers. НО. H₂ Pr Н- NH₂ To OCH 3 CH3 -OH -OH CH₂OH H₂CO H₂N H Pr CH₂OH -OH H-OH CH3 OH НО HO- Н- НО CHO -Н -H Br NC OH Br OH -Н CH2OH Н- Н- НО ... Br Br CHO -OH -OH -H L CH3 cast S NC OH
- 1. How are each of the structures A-F related to structure X? They could be E (enantiomers), D C (conformers), or I (identical). (diastereomers), CH3 CI -Br HOH₂C- -OH CI X НО, H3C H₂C D CI Br CH₂OH CI HO STEREOISOMERS Br A CH2OH CI Br CI HOH₂COH CI CI Cl CH3 OH E -CH3 -CH₂OH B Br Br НО. Br CH3 HOH₂C CI C CI CH3 HO CH₂OH F6. For each pair of compounds below determine whether they represent the same molecule, enantiomers, or diastereomers. CH H₂N H CH J OllinO 2||2 COOH C OH CH₂ OH NH₂ CH, COOH CH3 HO H₂N CH₂4 CH CCC COOH OH NH₂ NIIIIIC CH₂ H CH3 CH3 H₂N HO H₂N COOH CH OH 5- O J CH3 COOH O H CH₂ H COOH HO CH CH₂4 HOOC COOH ........ OH JCC H NH₂ NH₂ CH₂1a. How many stereogenic centers are present 1c. Draw a three-dimensional structure of a in the structure below? Indicate them with asterisk(s). How many stereoisomers stereoisomers are possible? chiral compound with the molecular formula of C4H4Cl₂ that does not have a stereogenic carbon. In addition, draw the enantiomer of this compound. Number of stereogenic centers: Number of stereoisomers possible: 1b. Draw one of the two most stable stereoisomers of the compound in 1a using a planar structure with wedges and dashes. Now draw it in its preferred chair conformation. 1d. Draw two meso compounds with the molecular formula of C7H14.