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- 4:30 PM Wed Apr 27 * 74% O O Q E HW 12 Home Insert Draw Layout Review View I| Select Objects Draw with Touch 40. There are five compounds with the formula C6H14 (one of them is linear and the others are branched). Draw structural formulas for any two of those branched isomers. See Example 6.3 on page 152. H3C CH3 CH3 44. Name the following alkanes. CH¿CH3 CH,CH3 CH3 CH;CH2CHCH2CH¿CH3 CH;CHCHCH,CH;CH3 CH;CHCHCH3 CH3 CH3 a C 3-CHhylheypare ethyl-2 methyllnexano а. 7+3 dimethibulane С. 46. Name the following alkenes. CH2=CHCH,CHCH;CHCH3 CH2CH3 CH2=CHCH2CH3 CH3 CH3 CH2=CHCH2CHCH3 a b C |burene а. b. C. 48. Name the following alkynes. CH,CH3 GH=CH CH3 C=CCH2CH3 CH;C=CCHCH,CH3 a b CWhat is the organic product? столосно NaOC₂H₂ H+ + CH-CH-C-OCHS CH+CH.C HOC₂H5 CH3 III. I. C₂H₂O CH O II. CH3-C CH3 CH-CH-C--OC₂H CH3 OH C₂H₂OCH CH O CH3-C-C-OC₂HS CH3 IV. C₂H₂O 0 CH3-C-C-OC₂HS CH39. Give the compound name, functional group name, and organic family name in each Ose. Classify alcohols as primary (1°), secondary (2 ), or tertiary (3"). Organic family Functional Formula Compound name group name CH3-CHz-CH-CH2-OH 1. CH3 CH,-CH,-0-CH,-CH,-CH, || CH,-CH, C-H CH CH,-C-CH-CH,-CH, CH-CH-CH- CH- COOH
- The enthalpy for hydrogenation of different isomers of butene is shown in the following figure. Which statement below best interprets this figure? Hy I3D H2 7k mot 5kJ mot + H2 AH-120 kJ mot AH"-127 kJ mot AH-115 kJ mot © GMU 2020 Stability and hydrogenation enthalpies are not correlated. Butene II is less stable than butene I by 7 kJ/mol. O Butene Il is 7 kJ/mol more stable than I and 5 kJ/mol more stable than III. Butene II is 5 kJ/mol less atable than butene IlI. Enthalpy7. H3C-CH The compound above is classified as a(n) alkane d. ketone alkene a. e. b. carboxylic acid c. akdehyde 8. Which of the follow ing is a secondary alcohol? d. CH3OH a. H3C C CH3 CH3 b. H3C0-CH3 e. CH3CH2OH c. OH H3C CH3 H. 9. CH3 OH -CH-CH-CH, H3C What is the correct name for the above compound? a. 2-methyl-3-butanol b. 2-pentanol isobutanol d. 3-methy-2-butanol none of these e. c.09:03 4G What is the correct IUPAC name for the following compound? .F "O. O A. 1-Fluoro-2,4-dinitrobenzene O B. Dinitrofluorobenzene O C. 1-Fluoro-4,6-dinitrobenzene O D. 1,3-Dinitr-1-fluorobenzene Add a caption... > Status (Custom) Z=O
- Using the average bond strengths below, estimate the molar heat of hydrogenation, AHhydrogenation, for the conversion of C4H6 to C4H10. CH₂=CH-CH=CH₂(g) + 2H₂(g) →→→ CH₂CH₂CH₂CH₂(g) || Bond C-H C=C H-H C-C kJ Bond Strength (kJ/mol) 413 614 436 348Write the names and draw the structures of the product/s formed from the reaction of 3-methylpent-2-ene with: 1. HBr 2. Cl2 3. H2O in the presence of H2SO4 4. Ethanol in the presence of H2SO4 5. Br2, H2O 6. [1] 9-BBN; [2] H2O2, OH-10.) (Name the following alkanes (IUPAC names). а.) Н-с —н H H H H Н-с -ҫ-с-с-с-ҫ-н H H H H H b.) I-C- CIH
- Order the compounds made of the following molecules by increasing melting point. но- molecule C (CH₂)7-CH=CH-(CH2)5-CH3 i HỌ–C—(CH2)7—CH=CH–(CH2)3CH3 i HO-C-(CH2)14-CH3 HO-C-(CH2)16-CH3 melting point (Choose one) 1 (lowest) 2 3 4 (highest) (Choose one) (Choose one) (Choose one)1. Consider the solubility and boiling point of the following pair of compounds: n-butyl alcohol and diethyl ether. The boiling points for the compounds are 118 °C and 35 °C respectively. The solubility for both compounds is the same (8g/100g water). Explain this observation for (i) boiling point disparity; (ii) solubility similarity a. H-bonds form in diethyl ether; n-butyl alcohol forms H-bonds in water b. H-bonds form in n-butyl alcohol; diethyl ether forms H-bonds in water c. H-bonds in n-butyl alcohol; Both compounds form H-bonds in water d. Both compounds form H-bonds; Both compounds form H-bonds in water 2. Account for the bond angle differences between (i) H-C-H (109.5°) in methane and H-S-H (90°); H-C-H (109.5°) and H-O-H (107.5°) in water. a. The H-S-H has two lone pairs; The H-O-H has two lone pairs b. The H-S-H has no hybridization at p-orbitals; The H-O-H has two lone pairs c. The H-S-H has two lone pairs; The H-O-H has no hybridization…1. Fill in the boxes with the missing reagents or major organic products for the alkene reactions. a. HCl b. H2O, H2SO4 с. d. 1. ВН, 2. H2O2, NaOH е. f. CI .CI g. Cl2, H2O h. 1. Н-О, Hg(OАс)2 2. NaBH4, NaOH i. 1. O3 2. Н:0, H-02 j. OH HO.