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A series of chemistry questions and answers, focusing on organic chemistry concepts such as hydrocarbons, functional groups, and reaction types. It includes questions about identifying compounds, understanding reaction mechanisms (like substitution reactions), and interpreting spectroscopic data (ir spectrum). The material is designed to test and reinforce understanding of key concepts in organic chemistry, providing a valuable resource for students studying the subject. The questions cover topics such as the identification of alkenes, the naming of dichloro benzenes, the identification of functional groups like esters, and the interpretation of ir spectra to determine the structure of organic compounds. The document also includes links to a periodic table, which is a helpful resource for students taking the exam. The questions are presented in a format that mimics an exam, with points assigned to each question and feedback provided on the answers.
Typology: Exams
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Click this link to access the Periodic Table. (https://previous.nursingabc.com/upload/images/Help_file_picture/Periodic_Table.pdf) This may be helpful throughout the exam. Hexene is a hydrocarbon containing (#) carbons and a (type) bond. Your Answer: 6 double C=C Hexene is a hydrocarbon containing 6 (#) carbons and a C=C double (type) bond.
Question 2 8 /^10 pts le.pdf) Click this link to access the Periodic Table. (https://previous.nursingabc.com/upload/images/Help_file_picture/Periodic_Tab This may be helpful throughout the exam. The compound below is what type of hydrocarbon? (Note: The question is not asking you to name the compound.) Your Answer: cyclohexene The compound below is a type of hydrocarbon called an alkene. minus 2 points; you provided the name and not the type.
This may be helpful throughout the exam. The compound below is called (term)- dichloro. Your Answer: 1, 3 - dichlorobenzene The compound below is called meta (term)-dichloro benzene. minus 2.5 points; meta
Click this link to access the Periodic Table. (https://previous.nursingabc.com/upload/images/Help_file_picture/Periodic_Table.pdf) This may be helpful throughout the exam. The compound below contains a/an functional group. Question 4 10 /^10 pts
Question 6 8 /^10 pts
Click this link to access the Periodic Table. (https://previous.nursingabc.com/upload/images/Help_file_picture/Periodic_Tab le.pdf) This may be helpful throughout the exam. The reaction shown below is a/an type reaction. CH 3 CH 2 CH 2 CH 2 CH 2 OH + HBr → CH 3 CH 2 CH 2 CH 2 CH 2 Br
Question 8 10 /^10 pts le.pdf) Click this link to access the Periodic Table. (https://previous.nursingabc.com/upload/images/Help_file_picture/Periodic_Tab this type of reaction is called SN alcohol → alkyl halide= substitution
This may be helpful throughout the exam. The following is a/an spectrum. Your Answer: IR spectrum
This may be helpful throughout the exam. The compound most likely to have given the SEM/EDS shown below is .
Question 10 7.5^ /^10 pts Click this link to access the Periodic Table. (https://previous.nursingabc.com/upload/images/Help_file_picture/Periodic_Table.pdf) This may be helpful throughout the exam. Which of the structural formulas below is likely for an organic compound,C 6 H 14 , whose IR spectrum is shown below? Note and assign at least 3 absorptions as part of your answer. a. CH 3 CH=CH-CH 2 CH 2 CH 3 CH 3 CH 2 CH 2 C≡CCH 3 b. CH 3 CH 2 CH 2 CH 2 CH 2 CH 3 c. The organic compound is (letter and type) The 3 most important absorption peaks and the bond deformationsthey describe are: Approximate peak location Bond The compound most likely to have given the SEM/EDS shown below is FeHCO 3 H is not detected by SEM/EDS
Your Answer: Organic compound is B, alkane Peak location and bond:
Which of the structural formulas below is likely for an organic compound, C 6 H 14 , whose IR spectrum is shown below. Note and assign at least 3 absorptions as part of your answer. a. CH 3 CH=CH-CH 2 CH 2 CH 3 CH 3 CH 2 CH 2 CH 2 CH 2 CH 3 b. c. CH 3 CH 2 CH 2 C≡CCH 3 The organic compound is B (alkane) The 3 most important absorption peaks and the bond deformations they describe are: Approximate peak location Bond C-H (stretch) 3000 - 2800 cm-^1 alkane (bend) 1450 cm-^1 C-H (bend) 1375 cm-^1 C-H