1) option B is correct
Explanation: Alkene attached to two substituents is called disubstituted alkene.
2) option C is correct
Explanation: Alkene attached to three substituents is called tri substituted alkene.
Chapter 8 1. What is the degree of substitution of the following alkene? golo com e...
Interaction of the following two atomic orbitals results in what kind of molecular orbital, in the orientation shown? + s bonding molecular orbital Op bonding molecular orbital Op* antibonding molecular orbital Which of the following is the correct structure for the compound (S)-3-methylheptane. B. D. A A OB Oc OD What is the degree of substitution of the following alkene? Monosubstituted Disubstituted Trisubstituted Tetrasubstituted Which of the following is a gauche conformer? Н. н Н Hн H Н. Н FH...
COH HOT A. Monosubstituted B. Disubstituted C. Trisubstituted D. Tetrasubstituted 7. Provide an IUPAC name for the following compound. IT Ans: en wollte bodo 13. Draw the structure of 3-methylcyclopentene. Ans: 15. Provide an IUPAC name for the following compound. Ans: 19. Is the geometry of the following alkene E, Z, or neither? HO- Ans: 22. Draw the Z isomer of 3,4-dimethyl-3-hexene. Ans: to lo
Which alkene would you e --Page 14 36. What would be the product of the following reaction? 0% 0% ーc d. IV e. All of these Which alkene would you expect to have the lowest heat of hydrogenation? a. CH2 CHCH2 CH2 CH-CH2 b. CH2 CHCH2
The E degree for the following react ion is 0.13V. What is the value of G degree (in kJ) for the reaction? Pb_(s) + 2H^+ Pb^2+ + H_ 2(g) (a) -25 (b) 25 (c) -12 (d) 12 (e) none of these
Chapter 11: 1. What is a prime rule in naming alkenes? a. Find the longest carbon chain. b.Find the longest carbon chain containing the alkene. c. Find whether the alkene has a cis- or trans- configuration. d.Find how far the alkene functionality is from either end. 2. What is the IUPAC name of the following alkene? a. cis-5-methyl-2-heptene b. trans-2-ethyl-4-hexene c. trans-5-methyl-2-heptene d. trans-3-methyl-5-heptene 3. What is the hybridization, geometry, and bond angle of the carbon marked by an asterisk?...
Sp17 03 V1 2) What are the substitution products of the following reaction? 2) CнзCH2Br Он- + A) CH3CH2BrH++O C) CH2-CHBr+ H20 в) СHзсH2он. Br- D) ноCH-CH2Br 3) Name the product of the following SN2 reaction: н а 3) OHT C) (A)-3-hexanol D) (S)-3-hexanol A) (R)-4-hexanol B) (S)-4-hexanol 4) Which of the following configurations corresponds to the structure below? 3 D) (4S, 5R) C) (4S, 55) A) (4R, 5S) B) (4A, 5R)
832 Chapter 38 Administering Medication G. Intradermal Injections 1. Answer the following regarding performing an ID injection. a. What size needle would be used? b. What is the maximum volume of medication given? c. What is the angle of the needle when administering the medication? d. What must be done to the site while inserting the needle? e. Where are the most common sites?
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
8. What is the major product of the following reaction? Cн, CH Cl (solvent) C сн, a сн, CH CH H OH H OH OH 9. What is the degree of unsaturation of C10H12N203? a 4 b.5 c. 6 d.7 10. Which of the following statement about using curved arrows in polar reaction mechanism is true? a. The nucleophile can be either negatively charged or positively charged. b. The electrophile must be neutral. c. Electrons move from a nucleophilic source...
9. Choose the most stable alkene among the following: a. 1-hexene b. (E)-2-hexene c. (Z)-2-hexene d. They are all of equal stability. 10. What is the relation between an enantiomer's configuration and its specific rotation? (a) R compounds usually are dextrorotatory with few exceptions. (b) R compounds always are dextrorotatory. (c) There is no relation. (d) R compounds always are levorotatory.