Which option is a correct representation of the missing information in Figure below? :O: :0: Il- CH3- CH2-C-Çi: -?- CH3- CH2-C- H-ö: A B sö: :0: CH3- CH2-C-CI : CH3- CH2-C-čI : H H. H H. D CH3-CH2-C-CI: CH3- CH2-Ci : H H. H А. А В. В С. С
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- 2H2O, H* X3 OH t°C HBr KCN H;C-CH-CH2-C ОН 1) X4 t°C 2) Но-СH2-С OH t°C 3) H3C-CH-CH2 CH2-C OH- с app.101edu.co Identify which of the following compounds is meso. I H₂CO H III H C H₂CO HCI Н A) 1 B) II Question 52 of 67 C) III D) IV OCH H₂CO "CH3 H C H CH₂ OCH₂ IV Н H₂CO H.C Н OCH, "H CH3 CH3 OCH₂ S В SubFor each organic compound in the table below, enter the locant of the highlighted side chain. CH3 - CH3 | CH₂ | C 1 CH3 - CH3 CH₂ — CH3-C CH₂- compound CH₂ - CH3 I CH CH₂- — CH₂ - CH₂ CH3 CH₂ 1 CH CH3 - - CH3- CH CH3 locant of highlighted side chain 0 0
- Identify A, B, C, and D CH3-CH2-C-CI so, AICI3 H,SO, B. Pd/H2 COOH Br For the toolbar, press ALT+F10 (PC)or AI TACNILEn1) Indicate chemically equivalent nuclei (e.g. Ha, Hb, Hc). 2) Estimate the chemical shifts on the following hydrogens. CH₂ OCH₂ O CH₂0 Br CH3-CH-CH₂-CH3 CH3 OH CH3-C-C=C-H CH3 C=C-H O H CH3 Br-C-C-CH3 H BrQ2: Choose the correct answer for each of the following: () 1 - In the infrared spectrum of a Compound containing a triple C-C bond, the amplitude oscillation band appears The Stretch) has at: - A) 2700 cm ¹ b) 2100 cm ¹ -1 c) 3100 cm ¹ 2- Stretching frequency of the O=C bond of a compound (3-butene-2-on) is less than the stretching frequency of a compound (2-propanone) a.) hydrogen bonding c) Vibration duplication b) Electronic effects 3- The compound o-hydroxybenzoic acid can be distinguished from the compound m-hydroxybenzoic Acid by infrared spectroscopy based on: a) OH. Group b) group curve oscillation) C-H c) group amplitude oscillation C=O
- Arrange the following classes of organic compounds in order of dereasing frequency for the C=O stretch. (NOTE: the dominant structural effect for amide is resonance while for ester and acylhalide, inductive effect). (b) (c) (a) CH,C-NH, CH,C-CI CH,C-O-Et CH,C-CH, CH,C-H (d) A. a>b>c>d>e (e) C. c>a>e>d>b B. b>a>c>d>e D. c>a>b>e>dFor each organic compound in the table below, enter the locant of the highlighted side chain. compound CH 3 | CH₂ - CH - CH₂ - C - CH₂ 1 1 CH3 - CH₂ I CH3 CH3 CH₂ CH3 t CH₂-C- CH₂ - CH - CH₂ CH3 CH3 1 CH3 CH₂-C- | CH3 CH3 locant of highlighted side chain 0 313) Designate the Cahn-Ingold Prelog priority order of the following C3H11- groups. (Lowest < Highest priority order) I CH:(CH;),- II (CH;);CCH,- III C;H;CH(CH;)- IV (CH;),CHCH,CH,- A)I< II < IIIFor each organic compound in the table below, enter the locant of the highlighted side chain. CH3 1 CH–CH–CH— CH CH3 I CH₂ CH3 I CH−C–CH−CH–CH–CH, | CH3 CH₂ 1 compound CH₂ I CH3 I CH3C-CH₂-CH-CH-CH₂ T CH3 T CH₂ | CH3 locant of highlighted side chain 0 0 0tps://app.101edu.co F2 910 # 3 + E F3 111 Compare the C-C bonds in the following structures: CH3-CH3, H₂C=CH2, HC=CH. Rank the C-C bonds in these structures in order from weakest to strongest. $ 4 R F4 ole in % 5 T Your Aktiv Learning trial expires on 05/23/23 at 12:59 AM F5 A) CH3-CH3 < H2C=CH2 < HC=CH B) HC=CH < CH3-CH3 < H2C=CH2 C) HC=CHChoose the structure below that must have given rise to the FTIR scan pictured below. Note that this particular scan was done as a KBr pellet. L00 FTIR 4000 H2N- OH H2N- он O CH;-(CH2 -C-H HO C C NH C CH3 CH2 OH NHSEE MORE QUESTIONSRecommended textbooks for youChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
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