Correct answer is
A— Secondary
B— Primary
C— Tertiary
Question 1 The molecule shown below is capsaicin which is an active component of chili peppers....
Exam 2: Name PROBLEM 1 (5 points) Capsaicin is the pungent component of various species of Capsicum, including red and green chili peppers, especially c. annum and is the active component of paprika. It has several actions in the body when ingested, such as stimulation of the formation of endorphins in the brain and increased salivation when eating spicy food. 1. The formula of capsaicin is Cy,Higo,N. A sample of capsaicin contains 6.79 x10 molecules of capsaicin. a. How many...
Identify the following statements as either True or False; the structures referenced are shown below. NH2 I H BIO B A is a primary amide Choose... C is considered an anti conformation Choose... - Stronger bonds will be found at higher wavenumbers in the infrared spectrum. Choose... - Choose... Dis a vicinal dichloride Acyclic alkanes have two fewer H atoms than cyclic alkanes with the same number of carbons. Choose... - Choose... Choose... - Compound E has primary, secondary, tertiary,...
Question 15 Use the reaction shown below to answer the following question. :NH ΕΝΗ + HO А B Choose the option that best describes the reactants A and B. А [Choose] Brønsted Acid Brønsted Base Nucleophile Electrophile B
1 through 5 please 1. Which level of protein structure is held together by hydrogen bonds only a) primary b) secondary c) tertiary d) quaternary 2. Which level of protein structure is held together by peptide bonds only a) primary b) secondary c) tertiary d) quaternary 3. Which level of protein structure is held together by R-group interactions? a) primary b) secondary c) tertiary d) quaternary " Which level of protein structure is likely to change when a substrate binds...
The structure of the antiviral drug oseltamivir (sold under the trade name Tamiflu) is given below. Answer the questions about this structure. Which orbitals are used for bonding by: Carbon A s p sp + p sp2 + p sp3 Carbon B s p sp + p sp2 + p sp3 Determine the configuration of the chirality centers, carbon atoms C and D. Carbon C R S Carbon D R S Which type of carbon is at the positions E...
Question 4 Use the molecule given below to answer the following question. 8 B Choose the option that best describes the VSEPR electron geometry of the indicated atoms. 1 (Choose ] Tetrahedral Trigonal Planar Linear EUR 3 5 [Choose) 6 [Choose)
Identify each functional group shown in bold letters. For each molecule shown below: 1) circle any bonds which have considerable polarity, 2) Indicate which atoms arc positive or negative, and 3) tell whether or not the overall molecule is polar The infrared spectrum of a molecule shows peaks at 3000, 1700, 1400 and 1200 cm^-1 Which of the molecules drawn in Part 3 would produce this spectrum? Explain how you made your choice. List each of these halides as primary,...
Which of the following functional groups is not found in the D) molecule shown in Figure 2? Он SH amide i) other iii) alkene iv) alkyne v) ester vi) thiol vii) i-vi are all present in the molecule R-0-2 NH Figure 2 E) Which of the following is not found in the molecule shown in Figure 3? но i) secondary alkyl halide i) primary alcohole ii primary carbon V quaternary carbon v) tertiary alkyl halide vi) tertiary alcohol vii)i-vi are...
ChemActivity 10: Oxidation and Reduction 145 Model 7: Primary (1°), Secondary (2°), and Tertiary (3°) Carbons The words methyl (0'), primary (1), secondary (2"), and tertiary (3) were used to describe the number of (nonhydrogen) R groups attached to a carbocation carbon (see CA 8). This same naming strategy is used to describe any carbon with one attached "heteroatom," Z (hetero other). H R Z any atom other than C or H (hetroatom) R- -z -Z н- alkyl (not H)...
ChemActivity 10: Oxidation and Reduction 145 Model 7: Primary (1°), Secondary (2°), and Tertiary (3°) Carbons The words methyl (0'), primary (1), secondary (2"), and tertiary (3) were used to describe the number of (nonhydrogen) R groups attached to a carbocation carbon (see CA 8). This same naming strategy is used to describe any carbon with one attached "heteroatom," Z (hetero other). H R Z any atom other than C or H (hetroatom) R- -z -Z н- alkyl (not H)...