Q: b) CH3 CH2-CH3 c)
A:
Q: CH,CH3 H,C CHCH2CH2CH3 H,C-C-CH3 H,C CH,CH,CH,CH,CH,CH,CH3 CH,CH3 a) b) c) ()
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Q: CH3 CH CI CH;CH2-C-C-CH3 ČHČI Br Br CH;CH; (4) (5) H CH;CH(CH;)2 CH;CH;CH3 (7) CH;CH2CH;CH3 Br…
A: General rule of IUPAC 1) longest chain is selected which consists of functional group. 2) For…
Q: 1ĄCHCH;ĊCH3 or CH;CH,CHCCH3 or CH2 CH3C-CH CH3 CH;C-CH CH3 or more less
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Q: Give the IUPAC name for each compound.
A: Rules for naming organic compound is as follows; Select the longest continuous carbon chain.…
Q: CH3 H3C N CH2 H2C-CH2 H3C (1) CH3 CH3 CH3 H2 Br CH3 CH2 ČH3 (2) CH HC CH CH
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Q: What is the configuration of each of the following?
A: The given compounds are represented as follows:
Q: CH3 CH3 CH3 CH, CH, CH2 CH3 CH, CH, CH, CH2 CH3C-ċ- D'I CH3 CH2 -CH-C-CH3 CH2 CH3 CH2 CH3 A
A: C will be the starting point. According to IUPAC nomenclature longest chain is selected. The…
Q: e). CH,CH2CHCH3 ci CH3 i). CH3-C-CI a). CH3CH2CHCH3 CI ci CH3 CH2CI b). CH3-C-CH3 f). CH3CH2CH2CH2CI…
A: * Two or more compounds having same molecular formulas but different structures i.e IUPAC names are…
Q: Draw curved arrows to show the movement of the electrons as the bond forms.
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Q: CI SN2 + HO CH;OH or CI SN2 + НО II CH3-S-CH3
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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: Convert each representation to a Newman projection around the indicated bond.
A: Newman Projection is a representation of showing three groups attached to one carbon atom on a…
Q: What is the major product of each of the following reactions?
A: The complete chemical equation for (a) is shown below.
Q: d. HC=C-CH(CH,CH,)CH,CH,CH, CH3 e. CH;CH2-C-C=CH ČH,CH,CH, f. CH,CH,C=CCHC=CCH3
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Q: Rank the following Newman projections in order of increasing energy.
A: Conformers can be defined as the structures of same molecule which are formed because of the…
Q: What is each compound’s systematic name?
A: In order to give the IUPAC name to the branched-chain alkane following steps are followed: The…
Q: CH3 CH2 CH3 CH; Ċ-CH, CH, CH, CH, CH2 CH, CH2 CH3 CH, CH CH CH2 ČH, CH, CH3
A: Alkanes are the compound that contains Carbon and Hydrogen atoms only bonded through single chains.…
Q: e) CHz CHz CH=CH2 CHz CH=CHCH3 and CH3 CH3 f) CH, CH CH2 CH2CHz CHz CHz CH CHz CH3 and :ö: g) CH3…
A: Resonance is the process in which delocalisation of negative charge or lone pairs occurs with…
Q: CH3 CH of o CH3 CI OCH3 CH₂CH3 Br CH3-CH-CH-CH2-CH3 1 H- H₂C OH O CH3 C—CH–CH2–CH3
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Q: d. HO CH₂CH-C3 NH₂ I 01 N-CHCH₂ OCH 3
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Q: a. CH;NHCH,CH2CH¿CH3 b. NH2 NH2 C. CH3 -N- d. CH,CH,CH3
A: a) CH3-NH-C1H2-C2H2-C3H2-C4H3IUPAC : N -methly -I -butanamine Namecommon name:…
Q: 5. (X)C,H¬OC1- NH3 →C¢H„ON- Br2 →CH3CH2CH2NH2; Compound (X) i : КОН CH3 (b) CH3 (a) (c) -HO- (d) cl-…
A: To solve this problem we have to complete the given chemical reaction .
Q: CH3 CH2OH CEN a. с. Br -ОН C. CH3 CH2NH2 b. CI OCH3 d. HOCH2 Br CI CH2NH2
A: In the letter E, the horizontal strokes are all on the same side; in the E isomer, the higher…
Q: H₂CHN +2 CH3MgBr followed by H + CH3NH₂ B+ NaOH +CH₂I +CH₂OH. H* E +NaNO₂, HC1-F + CH3COCI G -D A с
A: We have to draw the product of following reaction given below:-
Q: Which is the stronger acid?
A: (a)The hydrogen atom in CH3CH3 is attached to sp3 hybridized carbon atom whereas, the hydrogen atom…
Q: CH3 CI CH(CH32 А. DBN CH(CH3)2 "CH3 CH(CH32 CH3 CI CH(CH32 DBN CH3 CH3 CH(CH3)2 CH(CH,)2 B.
A: It is an second order elimination reaction. At first we have to draw the stable chair configaration.…
Q: CH3 CI CH₂CH3 +H -H CI A CH3- CI B CH3 CH3 CI H C C/ CH3 H D
A: Basic Rule to identify enantiomer: If configurations are R&S or S&R then the relationship…
Q: CH3 CH2 CH3 ČH ČH H3C. CH CH CH3 ČH3 ČH3 а. Br CH2-CH CH3 b.H3C CH3 H3C-C- CI ČH3 С. CH2 CH2 ČH CH…
A: IUPAC name of all the compounds are given below
Q: H. CH3 H. CH2CH3 H CH3 H. CH,CH3 H. H. CH3 H CH2CH3 H CH3 CH3
A: Projection 1 is the correct answer because when we see from C2 and C3 axis then it will form and…
Q: CH3 b. CHa CH2 CH =CC H2CH3 + CHo CH3 C CH3 CH = CHCHCH =CHCH3 CH CH3C HCH2 CH3 + d. CH3 CH2 CH2CH…
A: Organic compounds are named according to the rules and recommendations of IUPAC and these names are…
Q: CH3 H,SO, H,O intetndo saod H3C-CH=ċ-CH3 H3C-CH=CH2 + O2
A: The first reaction is a acid catalyzed hydration of alkene. In this reaction, acid acts as the…
Q: OCH2CH2CH3 a) CH;CH(OH)CHCH(OH)CH(CH:)CH3 H;C. но Br b) e) (CH3):CHCH2OCH;CH3 но. -CH3 CH3 c) bllege…
A: 1. We have to give the IUPAC names of the following given compounds as follows in step 2:
Q: A) CH;CH2OH + NaNH2 CH;CH2ONA + NH3. B) CH3CO2H NaOH CH;CO,Na + H2O + с) нC-CH + H2O NaOH HC=CNa +…
A: Given reactions are : For which of the following does the equilibrium favor reactants = ?
Q: H2SO4 CH;CHCH2OH CH3 H2SO4 2 CH,CHCHCH,CH3 CH3 Majo CHaCH-CHCH3 +2KOH Br Br
A: ->H2SO4 is a dehydrating agent which form alkene. ->Alco KOH is used for elimination reaction.…
Q: H;C. он CH2 Он CH3 CH2 H,C-C- CH3 CH2 он c) CH2 CH2 CH2 но CH2 CH2 b) a) H;C
A: Since you have asked multiparts questions, we will solve the first three sub parts questions for…
Q: Draw the skeletal structures for these two molecules:
A:
Q: CH3 CH3 B C A CH3 H Ph;P CH3 Ph3P CH,CH(CH3)2 Ph,P CH(CH3)2 D E F
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Q: , 2. 9. CH3 CH,CH3 CH,CH, C- CH-CH-CH,CH,CH,CH,CH, CH3 CH,CH,CH3 2.
A: IUPAC nomenclature is based on naming a longest chain of carbons present in a molecule which is…
Q: CH3 H3C CH3 (e) H2C=CHCHCCH3 CH3 (B) CH3CH2CH=CCH2CH3 CH3CHCH,CH3 (h) CH3CH2CH2CH=CHCHCH2CH3 CH3 CH3…
A: Given,
Q: (а) он он (b) он (C) HO CH3CHCH,CHPHCH9 CH2CH2CCH3 CH3 CH3 ČH3 CH3 (d) (e) H3C, он OCH3 Br Br Он
A:
Q: H3C CH3 a. N. b. CH3 c. CH3-CH-CH2-Ċ-OH с. d. CH3-CH2-CHBR-CH2-CHO CH3-C-NH–CH3 е.
A: During the IUPAC naming of a chemical compound, we have to remember the following main points --- i)…
Q: 4) CH3 H2C CH CH2 H2C CH2-CH CH CH3 5) CH2 CH2 CH2 CH2 CH2 CH3 CH3 6) CH2 H2C-CH2
A: Since you have posted question with multiple sub-parts, we are entitled to answer the first 3 only.…
Q: Name the following:
A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…
Q: (a) (b) .C. CH3CH2CH2 CH2CH2CH2CH3 CH3 H3C (c) H CH3 CH3
A: Esters can be synthesized by the reaction of alcohol and carboxylic acid in an acidic medium
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: А. B. C. D. HO w.. H3C CH3 CH₂ H CH3 CH3 CH3 CH3 HC3 CH3 HC3 CH3 Ž HC3 CH3 OH OH om CH3
A:
Q: 4. 5. 6. 7. Ст CH2CH3 OH OH H₂PO4 heat NO₂ OH PCC CH₂Cl₂ conc. HNO3.
A: Here we have to write the major product formed in the following given reactions. The major product…
Q: (i) CH3 CH2CI (h) (е) (g) BrCH2 CH2Br CH3 CH2COOH HOCH2 CH2OH CH3 CH2MG Br
A:
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- Propose structures for molecules that meet the following descriptions:a. Contains two sp2-hybridized carbons and two sp3-hybridized carbons.b. Contains only four carbons, all of which are sp2-hybridized.c. Contains two sp-hybridized carbons and two sp2-hybridized carbons.Using your model, construct an energy diagram to show the variation in the free energy of the molecule as the FRONT ATOM is rotated CLOCKWISE from 0º to 360º in 60º increments. In your energy diagram, you should clearly show the relative energies of each conformer.Compounds with several chiral centres may have configurations referred to as meso. Meso configurations arise when the molecule can adopt a configuration with an internal mirror plane. When this occurs, the mirror image of a molecule with an internal mirror plane is an identical configuration. Thus, even though the molecule may possess several chiral centres, they are reflection of each other (within the molecule) thus resulting in an achiral meso form. This occurs for example for tartaric acid (Figure 3.1). Because of this, tartaric acid only has three stereoisomers instead of four. It has the two chiral (R,R) and (S,S) enantiomers, and the meso form. Figure 3.1. Stereoisomers of tartaric acid. Given the information above on meso forms, how many different stereoisomers do compounds A to D (Figure 3.2) have? Figure 3.2. Structure of compounds A, B, C and D.
- Tamiflu(shown below) is an antiviral medication used to treat influenza. How many asymmetric centers are present in the this structure?Draw a bond-line structure that best matches the given 3D representation?The MOE results and a discussion pertaining to the conformation of Thioflavin T at low potential energies. At low energies, the conformation of ThT cannot be coplanar, that is, the dihedral angle cannot be 0. Why not?
- hi, can you solve this ? How many unbonded electrons are found around the nitrogen atom in the electron-point structure representation of the NH2 (-) ion?Propose structures for molecules that meet the following descriptions: Contains two sp2 hybridized carbons and two sp3 hybridized carbons.Propose structures for molecules that meet the following descriptions: (a) Contains two 〖sp〗^2-hybridized carbons and two 〖sp〗^3-hybridized carbons (b) Contains only four carbons, all of which are 〖 sp〗^2-hybridized (c) Contains two sp-hybridized carbons and two 〖sp〗^2-hybridized carbons