QUESTION 10 Select the correct number of primary, secondary, tertiary and quaternary carbons that are within the molecule shown here (You will need to make 4 selections) O 2 Primary O 3 Primary O 5 Primary 1 Secondary 2 Secondary O3 Secondary 1 Tertiary O3 Tertiary O 5 Tertiary O1 Quaternary 2 Quaternary 0 3 Quaternary
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A: The IUPAC name can differentiate the above-given compounds.
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A: The details solution for this is provided below in attach image.
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Q: H3C- -CH3 CH3 H3C CH3 Но ČH3 CH3 A B D H2N NH2 OH CH3 -CH3 -CH3 H3C- CH3 H3C- H3C CH3 H;C ČH3 F G H
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Q: QUESTION 2 Identify a to f CH3 CHCH,OH CH3 CHCHO PBr3 HCN b d H30* CH3 CHCH;MgBr
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Q: ОН ÇH3 ÇH3 CH3 H3C-O. `CH3 10 H3C-O `CH3 ОН This compound is called type your answer...
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Q: CH3 C(CH3)3 Br Br.
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Q: CH, CH,CH;NH CH4 CH;CH3 1 2 3 4 OH CH3 CH,CHGCHS CH,CHCHCH, CH,CH,CH,CH,CH,CH,CH, 6 7
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A: The IUPAC name of the compound is, 4,5-dimethylhept-2-yne
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- qor Br qom OH B -Br OCH₂ -OCH₂CH3The bond angles marked a, b, and c in the molecule below are about :O: H :O: || | || -CC-O-H a b c H H O 109.5°, 120°, 109.5° 120°, 120°, 90° 120°, 120°, 109.5° O 109.5°, 90°, 120° and respectively. [CLO-1]What is the order of increasing bond angles around the three indicated C atoms in the molecule? ΦΗ O B6-bromo-2,3-dimethyl-2-hexene Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. O 5 C O O 8 H 2D EXP' CONT. H N CI Br Marvin JS (1] A" by ChemAxon F AWhich structure is not a resonance form of the molecule M below? H₂N- OA O B C D M O E. None of these H₂N= H₂N= A 4 C EN: ●● H₂N- ** H₂N- O B D : 20 =N:CH₂CH₂CH₂CH=CHCH₂ Draw the molecules on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. H: 2D EXP. CONT I UZ O7. In each set of structures, arrange the labeltd bonds in the order indicaled Set 111 A to CHe CH2 H- C-H 12a bond angle . IncreasingIdentify the nature of bond and the appropriate orbitals involved in the formation of the bonds (#1-5) in the following molecule. H. H H C H C Bond 1 Bond 4 Bond 2 H C Bond 3 C Bond 5 t HHO S HNO3 H₂SO4Part 2 n indicates the exact number of neighboring Hydrogen atoms up to 3 sigma bonds away Example: isopropyl butanol daxww structure Fill in the table below: 4 Multiplicity (How many neighboring Hydrogens? D H₂C B V n+1 STIHO 1€ G CH₂ A B с Important! The Hydrogen of the OH group does not get split, nor does it contribute to splitting. D E F fecolantE Add 1 to the amount of neighbors. The result is the total amount of peaks in your signal. G I J Do not include the methyl group into your count, just the neighbors n=2 n+1 Signal name Signal appearance SIn the molecule shown below, determine which of the highlighted C-H bonds (from a to e) is expected to have the lowest bond dissociation energy Ha Ho Ho HD C-Ha B C-Hb C-Hc C-Hd C-He3. Which of the following molecules is nonpolar? O=C=O O Option 1 H-N-H :Z-H Option 3 Н * H-C-OH Option 2 HIC H HIC H O Option 4 Н H-C-C 0=0 O-H 1 pSEE MORE QUESTIONS