Q: Only question 64
A: Answer IUPAC and common name of the given compound
Q: H3 C CH2 CH2 CH CHZ CHz HO CH3 CH2 CHz
A: IUPAC - the standard way to.give the names of organic compounds
Q: (5) CHy CH --OH (k) CH 3 CH, NHCH, CH, a) CH,- CH2
A: The given organic entities exclusively consist of C, H and hetero atoms mainly oxygen and nitrogen.
Q: CH3 CH(CH32 H3C, H H
A: The structure of the above given compound can be drawn from the Newman projection given above,
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: H;C-0-H H;C-CH, H;C
A: order nucleophile :
Q: H H С—с—с—С—N -C- H. H H
A: FORMAL CHARGE RULE: Formal charge = No. of valance electrons - No. of non bonded…
Q: H,C-CH, H,C- -CH3
A: We need to provide correct IUPAC name for this 3D model of the molecule. For the first molecule: We…
Q: CH, CH,- -CH, CH CH, H,C- CH, CH, CH, CH, CH,
A:
Q: H H HH H-C-C-c=Ñ-H H H
A: Formal charge =Valence electron-negative(lone pair of electeon+1/2bondpair of elctron) Nitrogen has…
Q: Give an acceptable name for each compound
A: Since you have posted questions with multiple subparts, we will solve the first three sub parts for…
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: CH, — CH, — сн, CH, — CH, — сH, — С — сн, — сH, — сн, - CH,– CH, | CH3 CH — CH — СH,— | CH; CH,– CH,…
A:
Q: H H HH H |||| | H–C-C=C-C-C-H | H H H
A:
Q: i. H H,C-C -0 -CH,CH, j. H,C. он
A: A chemical reaction is one in which one substance (atom or compound) reacts with another substance…
Q: H,C HN-CH2 CH3 H2 C HC H2 CI H3C H2 CH.
A: The reaction is a nucleophilic substitution reaction.
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: CH3-CH2 C-N-CH3 + H H. H.
A:
Q: (b) H CH, H H H-C- -С —н Cl, + H H
A: The given reaction is an example of halogenation reaction
Q: k. H,C H CH -CH H,C CH2 CH, H. H. H
A: k) The name of the given alkene is, 3-ethyl-5-methyl-3-propylhexene l) The name of the given…
Q: HI H,C-0 -CH, `CH2 g. NH H,C H h.
A:
Q: H-NHCH,CH,CH3 CH;CH,CH,COH
A: When two reactants are allowed to react with each other in order to obtained the desired product…
Q: a. H-C-C-H
A: Ozonolysis is a quite important reaction in organic synthesis where unsaturated double bonds undergo…
Q: Calculate the formal charge on each second-row atom.
A: Formal Charge of an atom of the molecule is given by- F.C: Formal Charge of an atom. V.E: Number of…
Q: CH3 CH;CH,C-CHCH; HC/ZnCl2 ÓH CH3 I. CH;CHOH NaOH CH,
A:
Q: a CH,=CHCH,CHCH,CHCH, CH CH3 CH,CH, CH,C CCHCH,CH,
A:
Q: CH2 но — с — сН,. CH N. CH HN H. z-I
A:
Q: CH3 CI NH, .C. H3CH CH CH3 H2
A: The given compound name is 2-chloro-4-methylPentane. we know, the halides are the good leaving…
Q: CH2 CH, - CH, - C - CH, - C = CH, Br
A: According to IUPAC nomenclature, longest chain is chosen in such a way that if contains maximum…
Q: CH3 H,C=CH-CH,CHCH,
A: Selection of principle carbon chain Numbering Naming (PWS-prefix + word root + suffix)
Q: NH-CH; H,C-CH-CH,-CH; 3.
A:
Q: CH, CH2 CH3 CH5 C-CH, محاضرات د. ایر CH2 CH, CH, CH2 CH, CH2 CH, CH, CH, CH CH, CH3 CH, CH,
A: The systematic naming of organic compound is given by IUPAC. The naming of organic compound is done…
Q: CH,CH,CH,I -CH, H3CO
A: Since you have posted a question with multiple sub-parts, we will solve the first three sub-parts…
Q: g. Н-С-С CH,CH3 h. HICIH
A: A functional group is an atom or a group of atoms that are present in a molecule and is responsible…
Q: CHBr H,C + "OH C-C H, H,
A: Interpretation: We have to tell the products for the given reaction.
Q: Ph CH,-C=C-CH–CH, а. H.C CH3 C=C b. H c=c-CH,CH, С. (CH3);C-C=C-CH(CH;)CH,CH;
A: Alkynes is the class of hydrocarbons which contains a carbon-carbon triple bond and it is an…
Q: CH3 CH, — CH — CH, — сн, | CH; CH; CH, с— сн, — сн,— сн, CH, CH3 | CH, — сH, — сH, CH — сн, — Cн, —…
A: Step1 - identify the longest carbon chainStep2 - start numbering from that side such that senior…
Q: CH3 CH3 H CH, -c=c-C-CH, -C- H CH3 C -I
A: Naming of a compound is done according to the international rules set by IUPAC.
Q: CH3 H;C =CH,CH3 ČH3 CH3 ČH3
A:
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: 7. CH,CH,CH3 H,C CH3 ČH,CH,CH,CH, CH,CH,- -CH, 8. CH,CH
A: In order to write iupac nomenclature we have to follow some rules of iupac 1) first select longest…
Q: H;C-CH2-OH HO.
A: Primary alcohols are those in which hydroxyl group is attached to primary carbon atom. For example…
Q: CH CICH,CCH CH,CH(CH,), CH,CH,C- CHCH, CCH, Č,H, CH,CI CH3 H. OH H CHO CH, CHO
A:
Q: H3C. CH H,C- CH, CH, ČH CH CH3 HO но, OH H,C, H,C H3C H3C CH3 но HO но CH, но. H3C CH CH3 CH3
A:
Q: CH3 a. CH3-C-CH,CH,F c. (CH3),CCH,Br b. d. Br ĆI
A:
Q: CH3 H2 H3C-C-c-C- он H2 -C-CH3 اجابتك OH H3C он اجابتك
A: The IUPAC name of the given compounds has to be determined. a) b)
Q: H Mg H.C-C-I CH, b. H3C KCN C. CHO Na H,C CH, Ar
A: Since you have posted a question with multiple sub-parts, we will solve first three sub-parts for…
Q: CI CH,- CH, - CH -CH-СH,-CН, Br
A:
Q: CH, CH3 C=C CH, CH, CH,
A: select the longest chain of carbons (principle chain) numbering (it is done in such a way that…
Q: Name the following:
A:
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- Please ex plain and Please show all arrow pushing mechaarsas. Thank you!1. Draw the bond line structure for each compound (a. and b.) below 2. What are the fragment ions obtained for the following (a. and b.) through both the one bond and 2 bonds fragmentation pathways (Please show the steps in the pathways) a. (3E, 5Z)-2,5,8,9-tetramethyldodec-3,5-diene b. (CH3)3CCH2COCH(CH3)CH2CH3H8. Organic chemistry Text answers and (descriptive structures and / or reaction mechanisms). Explain the chemistry of the carbonyl group (direct addition of nucleophiles and addition with elimination)
- What 3 steps would be required to complete the following synthesis? Step 1 = A Step 2 3D в Step 3= B. NABH4, CH;OH C. PCC, CH;Cl; А. , AICI; D. CrO3, H3O* G. HNO;, H;SO4 J. i.propanal, ii. H+, H;0 K. NACN, DMSO M. Žn(Hg), HCI E. TSCI, pyridine H. CH;OH, H F. Bry, Light I. Brz, FeBr; L. i.butanal, ii. H+, H2O O. another reagent N. Mg. Et,0Preparation of para-iodonitrobenzene 1. Weight of p-nitroaniline = 0.552 g 2. Weight of para-iodonitrobenzene = 0.231 g 3. Theoretical yield = ............................................ 4. Percentage yield = ............................................. 5. Melting point range = .................... 0C.(a) Compound D undergoes a reaction with hydrogen bromide, HBr to produce 2-bromobutane. D exists as cis-trans isomers and decolourises bromine solution in methylene chloride, CH2CI2. Sebatian D mengalami tindak balas dengan hidrogen bromida, HBr untuk menghasilkan 2-bromobutana. D wujud sebagai isomer cis-trans dan memudarkan larutan bromin dalam metilena klorida, CH2CI2. (i) Draw and name the structure of compound D. Lukis dan namakan struktur sebatian D. (ii) Draw two (2) constitutional isomers of compound D. Lukis dua (2) isomer berjuzuk bagi sebatian D.
- It takes time to get the hang of R and S - and practice. For this activity determine R or S for each of the following molecules. Br H | 1. F H. 2. -Br C.. CI CH3 CN 4. L.CH, NH2 3. H CH3 POH CH II C COOH 5. C: H HOH,C & Instructions For each of the molecules determine R or S and give the groups in order of priority highest to lowest using greater than signs between them. So it would look like S, OH>NH2>CH3For 20.7 the solutions for part c and d dont seem right. Shouldn't reacting with 1 eq of H2 just take away the C=C bond and not the C=O bond. (H2 reduces C=C selectively to form a ketone according to page 738. Also the both the C=C and C=O bond should be reduced if excess H2 is usedWould you help me with these (5) Thank you.
- Consider the reactions below and the pool of choices. Reactant 1 Structure Choices: SAT Structure A MAT OH a Br WAT choose your answer... Concentrated H₂SO, RAT Structure B OH CAT Love NAT OH BAT OH Br The identity of Structure A is represented by the structure labelled OH choose your answer... Lo 16:21 while that of Structure B is labelled The missing reagent in the first reaction is choose your answer... ENC 3:35A. Electron-donating and Electron-withdrawing effects in conjugated structures 1. Go to the website http://molview.org/ 2. Draw the following structure on MolView. For each structure, obtain the following information: a. Charge b. Bond dipoles c. Over-all dipole Structure 1: Structure 2: H H. F F. Structure 3: Structure 4: Structure 5: Structure 6: You have to obtain the output from MolView. You can either copy the 3D image with the information, or you may draw them yourselves. Questions for Part A: 1. What are your observations based on the data you have obtained? 2. What can you infer about the nature of the substituents? Provide at least two inferences and explain your basis. 3. Which substituents is/are electron donating? Which of them are electron-withdrawing? 4. Which of the substituents is activating? Which ones are deactivating? Why do you say so? I0-2 3 5 [Review Topics] Reagents HBr a. b. C. H₂O, H₂SO4 d. Br₂ Cl₂ H₂, Pd Br₂, H₂O Cl₂, H₂O OsO4 then NaHSO3 e. f. g. h. i. j. k. I. [References] HBr, H₂O2, hv Hg(OAc)2, H₂O then NaBH4 BH3 then H₂O2, NaOH O3 then (CH3)2S m. n. O. p. q. r. S. t. u. V. 2 equivalents of NaNH₂ H₂, Lindlar's catalyst Na/NH3 H₂SO4, HgSO4 (sia)2BH then H₂O₂, NaOH 1 equivalent of NaNH2 NBS, hv Br₂, hv Cl₂, hv HCI Identify the reagents necessary to accomplish the following steps in the above synthesis of 3-hexanone from acetylene: Step 4: v Step 5: F Step 7: Previous Next Save and Exit