The answers for the questions 6, 7, 8 and 9 can be found in the images attached. As for the question no. 9, the molecular models are not provided. Other than that, all the structures given in the previous questions are named.
question 6b through question 9 please! thank you so much 6. a. Name each of the...
Week 10- Constitutional isomers Constitutional isomers have the same molecular formula, but their atoms are bonded in different orders. These may be further distinguished as chain isomers, which differ only in hydrocarbon chain structure, positional isomers, which differ in the location of a functional group, and functional group isomers which differ in the nature of their functional groups. Typically chain and position isomers show only modest differences in their physical and chemical properties, while functional group isomers differ greatly from...
If i could get some help on either of these 2 worksheets i would greatly appreciate it! Thanks so mich! do some molecules with the same formula (or even connectivity!) have different properties? ACQUIRE (USING MODELS!) 1. Fill in the following tables and BUILD each structure as you go. Have your instructor check your answers after each table or as directed Name and Condensed structure Skeletal structure Molecular formula Name: C8H18 2,3-dimethylhexane Molecular formula: C&HI8 Constitutional (structural) isomer of A...
Please help with the following: the structural formula of the isomer in step 2 of the procedure. Questions 3/4 of the procedure. Questions 2/3 of Analyze and Conclude Quick Lab Purpose To build ball-and Isomers of Heptane stick models and name the nine constitutional isomers of Procedure heptane 1. Build a model for the straight- chain isomer ofC Hes Draw the Materials structural formula for this isomer. ball-and-stick molecular 2. Remove one carbon atom from model kit (Colors used to...
H-CH Chloroalkane Isomers Molecular Formula Structure Compound Name Hн Hi-C-C-H Ethane CHO HH HCI CH,CI 1- chloroethane н-с-с-н HH CH 1,2-Dichloroethane C.H.CH H-C-C-H HCI Lab 10 Hydrocarbon Isomerism and Bond Rear 1 In step 3, does it matter which hydrogen atom on carbon 1 you choose to replace with chlorine Ty you get the same molecule or an isomer if different hydrogen atoms on carbon 1 are replaced with a atom? 2 In step 5, does it matter which hydrogen...
Lab 7. Molecular shapes. 3. Molecular Shapes Take a molecular model kit from the cart. Please read the cover of the kit and know what color represents which element. Black is used for carbon, while for hydrogen, green for chlorine, Also identify the bonds Short-grey used for single bonds. Long-grey used for multiple bonds. You can draw the three-dimensional structure of tetrahedral methane as: Solid lines: Bonds in the plane of the paper. Wedge: bond in front of page. Dotted...
please explain answers thank you (16) Write a chemical reaction for the complete combustion of cyclopentane, a its structure (not simply its molecular formula): te combustion of cyclopentane, and include (17) Calculate the oxidation state of the carbon atom for compounds sharing the molecular formula CH,O(show calculations): (18) Draw any two cyclic and any two acyclic structural (constitutional) isomers belonging to the molecular formula C&H N: HDI = C + 1 = 5 (H + X - N) (19) Draw...
help with these questions, I need clear explanations to understand 24. Name the following compounds. (6 marks total) a) Br Br Br c= c CH3 Br b) CH3-CH2-CH-CH2-OH OH 0 CH3-CH-C-CH2-CH2-F CH3 25. 26. Draw the structural formula for the following compounds. (6 marks total) a) 4,4-dichloropentanal b) 2-methylbutanol c) 3,3-dichlorohexane Draw and name all of the structural isomers that are ketones with five carbon atoms in its longest chain and the molecular formula C H, O. Can this molecular...
Thank you so much! (2 pts) Draw the major elimination products and Identify the mechanism responsible (E1 or E2). If both E and Z isomers form, only draw the E alkene. If only one isomer forms, label the alkene "E,""Z," or neither 1. NaOCH3 а. Br НОСHЗ b. НОСНЗ C. CI NaOCH3 d. (6 pts) Draw the substitution and/or elimination product(s) for the following reactions and identify 2. the mechanism responsible (SN1, SN2, E1, or E2) for each product drawn....
A. Enantiomers: Certain substances have the unique property of rotating the plane of plane-polarized light. Such light rotation is detectable with the aid of a polarimeter. In order for a molecule to be optically active it must be chiral. Chiral objects lack a plane of symmetry and are non-superimposable on their mirror images. A sp?- hybridized carbon atom can fulfill these requirements if all four of its substituents are different. 1. Methane a) Prepare a methane molecule and then substitute...
3. Cyclic compounds The presence of the ring in all but very large ring cyclic molecules prevents full rotation of the ring atoms. For this reason, stereoisomerism may also occur in cyclic molecules. a) Prepare a model of cyclohexane, C6H12. Draw the condensed formula. b) Build a model of methylcyclohexane (C7H14) by replacing one of the hydrogens of cyclohexane with a methyl group. Draw the skeletal formula for methylcyclohexane. 2 c) How many different isomers exist for methylcyclohexane (CyH34)? d)...