Chem 30B F2019 Practice Exam 2A 1. Which of the following compounds is a tertiary alcohol?...
Page 6 7 of 10 Chem 30B F2019 Pratice Exam 2A 21. Write the IUPAC (systematic name) of the following structure H "сH,сH, 22. Which of the following compounds is an hemi-acetal? OH IV A) I B) I с) ш D) IV E) More than one of these Page 7 Chem 30B F2019 Pratice Exam 2A
F10) Chem 30B F2019 Pratice Exam 2A 7. Draw the products of the following reaction of the hemi-acetal shown below with a catalytic amount of acid 人、“ 8. Draw a product from the following dehydration reaction (do not count water as a product). 9. What is the process called for the interconversion of one carbohydrate anomer (or B) stereoisomer to the other! 10. Circle the monosaccharides which are reducing sugars: TELY Page 3 Chem 300 F2019 Pratice Exam 2A
Chem 300 F2019 Pratice Exam 2A 14. The structure below is a-D-galactose. VO OH Identify the hemiacetal carbon atom in this structure (circle the correct letter). 15. Write the products of the following saponification reaction: CH-0--CH.CH.CH,CH O=0 CH-0- -CH.CH -0-C-CH.CH CHCH.CH, 16. Liquid oils usually have a higher percentage of what compared to solid fats? A) Oxygen B) Hydrogen C) Unsaturation D) Aromatic rings
Name Worksheet Alcohols, Aldehydes, Ketons 1. Circle the molecule which will have the highest boiling point: CH,CH2CH3 CH2=CHCH, CH,CH2-OH 2. Classify these alcohols as 1º,2º, or 30: OH CH3CH2CHCHCH2CH2-OH: C1 CH) 4-choloro 3-hexene HH OHH H-C-C-C-C-H Η Η H H-C-H CH3CHCH OH 2-propanol H 3. Name each of these alcohols: CH,CH2CHCHCH2CH2-OH CH CH3CH2-OH Ethyl alcohol HH OHH H-C-C-C--H Η Η H H-CH CH,CHCH OH H Aldehydes and Ketons nonsolo 4. Give the IUPAC names for the following aldehydes: OH O...
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250 Chapter 9 Chapter 9 Practice Test Which of the following reagents is the best one to use in order to wing reagents is the best one to use in order to convert methyl alcohol into methy bromide? 2. Br HBr Br NaBr Br* a. what would be the major product obtained from the reaction of the epoxide shown below containing 0.1 M HCI? CH2CH; CH CH3 b. What would be the major product obtained from...
a) tert 14. Which of any alcohol upon reaction with methylmagnesium Which of the following compounds does NOT give a tertiary bromide? CH, HC CH₂ D - Η Β) 10. Which of the following compounds is NOT oxidized by pyridinium chlorochromate (PCC)? a) 2-methyl-2-butanol b) 1-pentanol c) 2-pentanol D) 1,3-propanediol 11. What is the complete systematic IUPAC name for the following compound? A) 4-(1-methylethoxy)-4-isopropyl-4-methylpent-2-cne B) 4-isopropyl-2,4-dimethylhept-5-en-3-ol C) isopropyl-(4-isopropyl-4-methylbut-2-enyl) ether D) 4 isopropoxy-4,5-dimethylhex-2-ene E) 4-isopropyl-4-methylbut-2-en-isopropyl ether 12. Which of the following...
commond in PRACTICE SHEET NH2 04/04/2018 OH a. Which H is the most acidic ? (circle it) b. What product forms when the compound is treated with HCI ? (Draw it above) c. How many sp3 hybridized carbons does this molecule have? d. How many H's are on the attached to the N? 10 a. Indicate the strongest IMF available to each of the compounds below. Oligo H A B b. Which compound would you expect to have a greater...
26) Name the following compound. CH3 H2C=CH-CH2CHCH: A) 1,1-dimethyl-3-butane B) 4-methyl-1-pentene C) hexene D) 2-methyl-4-pentene E) 2-methylpentene 27) Name the following compound. CI A) 2,3,5-trichlorobenzene B) trichlorostyrene C) 1,3,4-trichlorobenzene D) 1,3,4-trichlorohexene E) 1,2,4-trichlorobenzene 28) Identify the formula for an alkene. A) CnH2n+4 B) CnH2n+2 C) CnH2n D) CnH2n-4 E) CnH2n-2 29) Name the following compound. A) 1,4-bromocyclohexene B) 1,4-dibromobenzene C) 3,6-dibromobenzene D) 2,5-dibromobenzene E) 2,5-dibromocyclohexene 30) Name the following compound. CECH CH,CH,CHCH A) 2-ethynebutane B) 3-methyl-1-pentyne C) 3-methyl-4-pentyne D) 3-ethyl-1-butyne...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...