My answer was A and B but it was incorrect
Constitutional (or structural) isomers differ in the order in which the atoms are connected together so they contain different functional groups and/or bonding patterns (e.g. branching). In the given problem. Remember they have the same molecular formula but different structural formula. So option C is clearly ruled out(as it depicts C4H10).
Option D is the same molecule with the same chain structure.So, it is also ruled out.
The remaining options A,B,E and F contain stereoisomers of the given molecule.
My answer was A and B but it was incorrect Incorrect. C-H Identify any structure below...
Please answer the questions 1. 2. 3. CI H НН Identify any structureis) below that represent(s) another representation of the compound shown above. Do NOT select any constitutional isomers of the compound above. Select all answers that apply. H C НН CI H НН H C A. D C. none of the above
Klein, O identify any structure(s) below that represent(s) another representation of the compound shown above. Do NOT select any consttutional somers of the compound above. Select all answers that apply. C. B. D. 3/2018 here to search
9 Considers the three compounds shown below and then answer the questions that follow: H H H H 日 - CHA HC - HK # H: iii H H H H Compound A Compound B Compound C a) Which two compounds are constitutional isomers? b) Identify the compound with the fewest number of o bonds. c) Identify the compound with the greatest number of o bonds. d) Identify the atom containing a trigonal pyramidal geometry.
9. Considers the three compounds shown below and then answer the questions that follow: H H H H H H H N-CH3 H H C N H H: C C H: [ C CSN H HC C H H H H H H H H H Compound A Compound B Compound C a) Which two compounds are constitutional isomers? b) Identify the compound with the fewest number of o bonds. c) Identify the compound with the greatest number of o...
Which compound is a constitutional isomers of the structure shown here? 5. Which compound is a constitutional isomer of the structure shown here? A) B) C) D)
My current answer is incorrect Ch. Ex. 84 - Oxidation - use aldehyde product structure of identify and draw alcohol reactant 5 attempts left Check my work Click the "draw structure" button to launch the drawing utility. Draw the alcohol that would be oxidized to form the aldehyde shown below. CH2CH edit structure...
1. (6 pts) A compound has a molecular formula of CHO a. Draw a structure of a compound with the above formula that contains an ether group and one chirality Center b. Draw the structure of an ether that is a constitutional isomer of the compound drawn in part above 1 c. Draw the structure of a constitutional isomer of the compound drawn in part (a.) which contains a different functional group.
A. (b) Identify structure(s) for all constitutional isomers with the molecular formula C4Hg that have one double bond. Select all that apply. H H H C. H C - 0- 0- 0- H H-CC=C—CH H H H H. H H H H -6-I || IT Itt I H H I- B. H C - C= C- H H- C= C— C— C— H - 0-II II HHHH HC-H Which of the following is a constitutional isomer of cyclopropane? н. Н...
9. Which of the following is not an isomer of hexane? 1. 2,2-dimethylbutane 2. 2,2-dimethylpentane 3. 3-methylpentane 4. 2-methylpentane 5. 2,3-dimethylbutane 10. Ascorbic acid (vitamin C) is not a carboxylic acid, but rather has the structure shown below. How many stereoisomers of this compound are possible? НО. 0 ascorbic acid HO но OH a. 1 b. 3 c. 4 d. 6 II. Short Answer Questions. (70 pt total) 1. a. Identify the functional groups in the following molecule as circled....
4.) a) (10 pts) Consider the three constitutional isomers of dioxane (C&H:02): One of these constitutional isomers (Isomer A) is stable under basic conditions as well as mildly acidic conditions and is commonly used as a solvent. One of these (Isomer B) is only stable under basic conditions but undergoes hydrolysis under mildly acidic conditions. The remaining isomer (Isomer C) is extremely unstable and potentially explosive. Identify each isomer (label each as A,B or C) and explain the properties of...