(61-65) For each of the hydrocarbons on the left, select from the response list on the right the correct molecular formula. Responses on the right may be used more than once or need not be used at all. 61. 2,3-Dimethyl-2-pentene a) C>Hg b) C;H10 62. 1,3-Heptadiene с) СH12 d) C;H14 63. 3-Неptyne 64. 2-Methylcyclohexene 65. Toluene

(61-65) For each of the hydrocarbons on the left, select from the response list on the right the correct molecular formula. Responses on the right may be used more than once or need not be used at all. 61. 2,3-Dimethyl-2-pentene a) C>Hg b) C;H10 62. 1,3-Heptadiene с) СH12 d) C;H14 63. 3-Неptyne 64. 2-Methylcyclohexene 65. Toluene

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

12
5. What is the IUPAC name for the molecule shown below? a 6-methylhepta-2,4-diyne b 6-methylhexa-2,4-diyne c 6-methylocta-2,4-diyne d 6-methylpenta-2,4-diyne
QUESTION 27 Cyclohéxanone plus sodium borohydrate yields O cyclohexanal O pentanoic acid and CO2 O A six carbon dialdehyde O cyclohexanol O A six-carbon diacid QUESTION 28 Which cycloalkane relieves most of its ring strain by undulating the flap of a "puckered" e O Cycloheptane O Cyclopropane O Cyclohexane O Cyclobutane O Cyclopentane
Which corresponds to the best answer?
1- Draw each of the following organic molecules: a) 2,6-dichloroaniline b) 3,5,7-triethyl-4,5-dimethylnonane c) trans-3-methyl-1-phenyl-2-hexene d) 2-fluoro-4-isopropyl-5-pentylphenol e) 4,5,7-trimethyl-3-octyne f) 3,3,5,5-tetraethyl-4-heptanol g) 2,4-dibromo-2-methylpentanal h) 1,1,1,3,3,3-hexachloropropanone i) potassium 2-cyclobutylbutanoate j) tripropylammonium benzoate h) cyclopentyl ethanoate i) octanoic acid j) N-2,6-triphenylnonamide k) cyclopropyl isopropyl ether
Can u answer both please
please answer 6, 7, 8
Question D
10) What is the name of the major organic product of the following reaction? CH2=CHC(CH3)3 H*, H₂O A) 2,3-dimethyl-1-butanol B) 4-methyl-2-pentanol C) 3,3-dimethyl-1-butanol D) 2,3-dimethyl-2-butanol E) 3,3-dimethyl-2-butanol
estion 12 of 33 Write down the common (not IUPAC) names of the organic molecules that would be released if this molecule were hydrolyzed: 0 CH2-0-C-(CH2)16-CH3 о о O= = = CH-O-C-(CH2)4-CH=CH-CH2-CH=CH-CH2-CH=CH-(CH2)4-CH3 Separate each name with a comma. You will find useful information in the ALEKS Data resource. Question 13 of 33 Write down the common (not IUPAC) names of the organic molecules that would be released if this molecule were hydrolyzed: CH₂-01 CH-O ང CH₂-01 Separate each name with a comma. You will find useful information in the ALEKS Data resource. Question 14 of 33 Draw the skeletal ("line") structure of the triacylglycerol that could be formed from lauric acid.
Only 5 th
Identify the carbon atom that should be designated as #1 when naming this compound systematically. CH3 Which carbon is C1? A E A -CH2CH3 H3C D E Give the systematic name for the compound. Spelling and punctuation count! Name: