Q: CH2CH3 H2C=CHCH=CH2 CH2CH3 CH3 CH3
A: The IUPAC name of an alkene consists of three parts: rootname, prefix and suffix. The carbon atom…
Q: CH,C=CCH=CHCO2H CH3CHCH2CH2CHCH3 CH3 CH;CCN CO2H CN .CO2H NC
A: These given compounds are consist of several functional groups. It is very important to choose the…
Q: CH-C-CH, C. CH2CH2CH2-C-CH,CH2--CH3 CH2CH3 (d) d.
A:
Q: 5. 다음 거울상 이성질체 각 탄소의 R과 S를 결정하시오. (a) (b) (с) но. ОН H. „CH3 CH3CH2 H. H3C CH3 ----
A: We have to determine the R and S of each of the following given isomer in the mirror as follows in…
Q: CH;CH2CH3 d. CHg-CHCH2-C-CH3
A: Iupac name of alkane depand longest possible carbon chain
Q: Provide methods for preparing the following compounds by the Grignard method:
A: The given compound can be prepared by using Grignard method.
Q: CH3 CH3 11 |13 12 2 10 8, 14 3 4 6 7 a) Substituent Up at C4. b) Substituent Up at C11| c)…
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Q: (а) (b) Br (c) FoH CH3CHCH,COH CH3CHCH2CH,COH CH3CH-CHCH,CH2CH3
A: Since we only answer up to 3 subparts, we will answer the first three only. Kindly resubmit the…
Q: (d) CH2CH3 CH3 (e) CH3 CH2CH3 (f) H3C CH3 CH3CH2CHCH2CH2CHCH3 CH3CH2CH2CHCH2CCH3 CH3C-CCH2CH2CH3 CH3…
A: For IUPAC naming select the longest chain and the longest chain must contain maximum number of…
Q: 3(R),4(R) 3-Bromo-3,4-dimethylhexane CH2CH3 Br -CH3 NaOCH3 in CH3OH heat -CH3 CH2CH3
A: There are 3 products possible from the elimination reaction of 3(R),4(R) 3-bromo-3,4-dimethylhexane.…
Q: Indicate how you could distinguish between the following pairs of compounds by using infrared…
A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…
Q: Label the sites of torsional and steric strain in each conformation.
A:
Q: CH3COCH3 is more reactive than CH3CHO towards HCN. True False
A: Aldehydes(CH3CHO) and ketones(CH3COCH3) undergo nucleophilic addition reaction with HCN, where CN-…
Q: Identify compound Y? Ha B12 Y CH3 CHa Lindlar Pd
A:
Q: Give the mechmisam amd chooe corsect optiom? CH2I2 H2 (2) (3) IH2C (4)
A:
Q: [References] Rank the set of substituents below in order of priority according to the…
A: The substituents given are, a) -CH=CH2 b) -CH(CH3)2 (c) -C(CH3)3 (d) -CH2CH3
Q: CH2• А) CH3CHCH2CH3 CH3 B) CH3CHCH2CH2• CH3 C) •CH2CHCH2CH3 CH3 CH3CHCHCH3 D) CH3 CH3CCH,CH3 E)
A: Stability of radical is based on +I effect and hyperconjugation. Greater is the no. of +I effected…
Q: heat CH;CH2CH2CH2CH2CNCH2CH3 + H,0 + HCl CH2CH3
A: The given reactant is an 'Amide' & the reaction takes place would be Acidic hydrolysis of Amide.…
Q: Rank the following groups in order of decreasing priority. −NH2, −CH2NH2, −CH3, −CH2NHCH3
A: Priority is given to elements on the basis of atomic numbers. If the atomic number is more, its…
Q: three-dimensional line structures of (2S, 5R)-5-amino-2-hydroxylhexanal. Clearly show the…
A:
Q: 7. CH3(CH3)CH=CH2 3. CH3CH2CH2C(CH3)=C(CH3)CH2CH3 э. СНЗCH2CH(CHз)C-CH 10. CH3CH=CHCH2CH=CH2
A: “Since you have posted a question with multiple sub-parts, we will solve first three sub-parts for…
Q: ए्कच्टे ने मैंकट (तनेक्जकास्ीवेच्ळ फीकह0 ड कळ्ड़ी एळत्जे वनी नhe TTECAवकांडण नि गीए जख्तंपरमीं ०1 ी…
A: ->LiAlH4 is reducing agent as it can produce hydrogen anion (hydride ion) which can acts as…
Q: ch3ch2(ch3)ch2ch(c=o)ch3 pka value
A: For a general reaction: HA <=====> H+ +A- ka = [H+] [A-]/ [HA] And pka is defined as follow…
Q: 4. For each pair state whether the two are a) the same molecule, b) different compounds that are not…
A: On the basis of configuration of chiral centre we decide stereo of following molecule .
Q: Options: A CH3COOCH3 B CH3COOH C CH;CONHCH2CH3 D CH3COCI E CH3COCH3
A:
Q: Give the tupac name for the following compound CH3 CH2 ÇHCH2 CH2CH3 CO,H C=C H3C CH2 CHz COH
A: Interpretation - To write the IUPAC name of the compound which is given in the question .…
Q: Dieckmann- Condensation A В C Keton タール Ph-COCI E H2O/H D F - H20 - HCI (SN) 1,3-Diketon
A: This reactions are bassed on electrophilic nature of carbonyl carbon. Thats favour the nucleophilic…
Q: a. H,O H,SO,, + Pt catalyst b. C2H5-CEC-H + H2 UV light C. CH:CH2CH2CH2CH3 Cl2 CH;=CHCH,CH,CH,CH; +…
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Q: 2. Which is the appropriate conversion of CH3CHCICH2CH(CH3)2 to a skeletal structure? b. d. a. А. А…
A: Skeletal structure for above compound
Q: i. H* H3C-C-o-CH2CH3 H,0 j. H" о-н + H3C- HO- H3C
A: The given two reactions are hydrolysis of ester and esterification of carboxylic acid.
Q: Fisher Ball-and-stick Haworth Chair/ Envelope Conformation [2] Complete name Projection structure…
A: Ans. [1]α-D-mannopyranose: Ball-and-stick structure [2] Chair/envelope conformation: [3]…
Q: VI. Give IUPAC names for the following compounds: (c) (a) CH3 (ы) он он HOCH2CH2CHCH20H…
A: IUPAC name of the given organic compounds are -
Q: OH H30* (d) CH3-CH-CH2- ċ-CH2-CH3 A 9. OH H30* (е) CH3-C-CH2-C-CH3 ČH3 OCH3 (f) CH30-C-CH2-C-OCH3 +…
A: In presence of H+ and heat , alcohol compound undergoes E1 elimination through carbocation…
Q: What is the absolute stereochemistry of C2 and C4?
A: The asymmetric carbon is categorized as chiral center. Its configuration is determined by using…
Q: C2H4 + CH3CH2LI produce: O C2H4+Li+ CH3CH3 O CHCLI + CH3CH3 O C3H6 + H2 O C3H5LI
A: Given reaction is : C2H4+CH3CH2Li→?
Q: 2.) Which is a pair of enantiomers? CH3 H3C CI ČH;CH;CH3 CH3 CH3 CH;CH;CH3 H3C CI CH;CH2CH; II II…
A: Enantiomers are chiral molecules which are the non superimposable mirror images of each other.…
Q: 46) E cHg + NH, ËN HNH, CH3 (CHz)+ どHNH。 47) CH3 (CH2)4 ECH + cHtz eHq NH 48) (cH3)2 CHz CH,C OfH 4…
A:
Q: CH3 H3C CH3 (e) H2C=CHCHCCH3 CH3 (B) CH3CH2CH=CCH2CH3 CH3CHCH,CH3 (h) CH3CH2CH2CH=CHCHCH2CH3 CH3 CH3…
A: Given,
Q: Which method-Grignard carboxylation or nitrile hydrolysis-would you use for each of the following…
A: Since you have asked a question with multiple sub-parts, we will solve first three sub-parts for…
Q: (b] CH3 CH3CHCH2CH2CІ {e) I CH2CH2CI CH3CHCHCH2CH3
A: Give the IUPAC name of the given structures-
Q: CH2 H2C CH3 CH C-CH3 H2C CH ČH3 CH3-CH-CH3 CH2=CHCH2CH=CHCH2CHCH3 CH3 CH3 HÖCH2CH2CCH2CH2CH ČH3
A: Bond-line structure also called skeletal structure. In molecular structure the covalent bonds are in…
Q: How would you carry out the following transformation? Tell what reagents you would use in each case.
A: NOTE: “Since you have posted a question with multiple sub-parts, we will solve first three…
Q: Name the following structures: CH3 OCH3 CH3CH2CHSH HOCH2CH2OH CH3 OCH2CH2CH3 CH3CHSCH2CH3
A: We can write name of a compound by following iupac rule . 1.First of all select longest carbon chain…
Q: (T) CH3 (d) CH2CH3 (e) H2NCH2CH2CHNH2 CH3
A: The IUPAC system is the most widely used system of nomenclature in organic chemistry. There are…
Q: lowing Compounds cl CHY 9) DA en O uDE -c Hz-CHz=cHz-c= LODA OMIDE LEB HEEL ーCH-C-Cる CHz DV…
A: Given : We have to write the IUPAC nomenclature for the given compounds.
Q: OCH3 CH3 CH3CCH3 CH3CH-0- ÓCH3 CH3 CH3 SCH3 -SCH3 CH3CH2CHCHCHSCHCH3 ČH3 ČH3 SH -CH3 `NO2
A:
Q: O || CH3CH₂-C-H A) CH3CH₂CH₂CN || C) CH₂CHCH CN HCN CN -? B) CH3CH₂CHC=NH OH D) CH3CH₂CHOH T CN
A:
Q: II CH3-CH2-CH2-CH Butanal CH3 CH3 CH2 CH3 0 II CH3-C-CH,– CH3 CH2-CH CH3-CH-CH CH2 =C- CH3 A B D
A: The structure that is not an isomer of butanal has to be determined.
Q: A CH3COOCH3 B CH3COOH C CH;CONHCH2CH3 D CH3COCI E CH3COCH3
A: Option A is correct
Q: Chemistry FII CH3 Br FF CH3 CH₂CI B I flera H₂N CH3 H H₂C CH3 OH Determine the absolute…
A:
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- Rank the following groups in order of decreasing priority. −NH2, −CH2NH2, −CH3, −CH2NHCH3Lithocholic acid is an A–B cis steroid found in human bile. Draw lithocholic acid showing chair conformations, as in Figure 27-11, and tell whether the hydroxyl group at C3 is axial or equatorial.Rank the following groups in order of decreasing priority. −CH=CH2, −CH3, −C≡CH, −H
- Rank the following groups in order of decreasing priority. a. – COOH, – H, – NH2, – OH b. – H, – CH3, – Cl, – CH2CI c. -CH2CH3, -CH3, -H, -CH(CH3)2 d. – CH = CH2, – CH3, – C ≡ CH, – HRank the following groups in order of decreasing priority. −F, −NH2, −CH3, −OHpls show the the isomers of butane-2,3-diol. Which pairs are enantiomers? diastereomers? mesomers? pls explain why
- Rank the following groups in order of decreasing priority (1 = highest, 4 = lowest)Rank the following groups in order of decreasing priority. a.−F, −NH2, −CH3, −OH b.−CH3, −CH2CH3, −CH2CH2CH3, −(CH2)3CH3 c.−NH2, −CH2NH2, −CH3, −CH2NHCH3 d.−COOH, −CH2OH, −H, −CHO e.−Cl, −CH3, −SH, −OH f.−C≡CH, −CH(CH3)2, −CH2CH3, −CH=CH2For the given ee values, calculate the percentage of each enantiomer present.a. 90% eeb. 99% eec. 60% ee
- a) Draw a 2-dimensional structure of 4,5-dibromooctane and label, with an asterisk, thetetrahedral stereo centers.b) What is the maximum number of stereoisomers for this molecule?c) Draw Fischer projections of all the potential stereoisomers of (a).d) Label, on the above projections, all the stereocenters as R or S.e) Indicate the enantiomers, diastereomers and the meso compound if present.Use Apendix C or Figure 18.9 to determine whether Kc > 1 or Kc < 1 for each reaction. (a) H2SO3 + NH3 HSO3- + NH4+ Kc < 1 or Kc > 1 (b) HCN + HCO3- H2CO3 + CN - Kc < 1 or Kc > 1Which group in each pair is assigned the higher priority? a. – CH3, – CH2CH3 b. – I, – Br c. – H, – D d. – CH2Br, – CH2CH2Br e. – CH2CH2Cl, – CH2CH(CH3)2 f. – CH2OH, – CHO