5) Provide your own list of alkanes. They can not be the same structure but should all have the same number of carbons. (see the problem solving video for an example) Rank them in order of increasing melting point. You can not have the same example as someone else.
Q: trans-1,2-dimethylcyclohexane
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Q: hich of the following represent structural isomers of the molecule shown in the model? Choose all…
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Q: Now, if you take the above compound, and place a METHYL group on the carbon in the BACK LEFT…
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Q: What are the peak positions, bond types and functional groups?
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Q: Give 3 great examples of branched chains of alkane,alkene,alkyn. See image for sample.
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Q: Use these bonds and atoms to do the following: 1. Construct a model of methane. Write down its dash…
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Q: What is the name of the IUPAC compound shown here? (see attatchement) First time you guys…
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Q: Figure 4 A B C D Br Br
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Q: Identify all functional groups in the structures below. Make sure to circle and label each of them.…
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Q: Examine the cycloalkane above. There are two carbons that make up the front of the ring, and three…
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Q: how you can determine which of the following compounds might be alkanes, cycloalkanes, alkenes, or…
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Q: For this problem, please draw skeletal structures for the following two molecules (you will have two…
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Q: 8. Circle and identify the functional groups in the molecule below. Ignore all alkanes. NH
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Q: What is the smallest straight-chain alkane that is a liquid at room temperature (which is about 25…
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Q: Directions: Identify the functional group each compound represents. If the compound represents two…
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Q: How many additional 3-atom resonance forms can you draw for the alkane shown in the picture…
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Q: A carbon skeleton for cyclohexane is shown below. Where on that skeleton would the substituents be…
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Q: You have a laboratory bottle containing an organic liquid that is suspected to be alkane or alkene,…
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Q: What are the peak positions, characteristics, bond type and functional groups?
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Q: Draw an alkene and an alkyne, using R groups for both. On both structures, please indicate the…
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Q: 2. How many distinct types of carbons exist on the compounds below?
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Q: Are they isomers? Yes or No If yes, Structural What kind OR Stereo?
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Q: Draw out and name all the alkene isomeric structures for C4H8 (Hint there are four) Draw and label…
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Q: Draw all the structural isomers for the molecular formula C,H,Br. Draw all hydrogens.
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A: The solution of the question is given below:
Q: Based on the structures of these three molecules (3,3-dimethylbutan-2-one, 4-methylpentan-2-one,…
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Q: 2. Draw and label displayed formulae for the E and Z isomers of 1,2-dichloroethene.
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Q: Name the alkyl group as if the dashed line were where it was connect to the rest of the molecule,…
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Q: 1,3-dimethylcyclohexane and Cl2 forms what?
A: Reaction shown below:-
Q: the subject is naming alkanes. I need to understand when to name something by sec, tert... for…
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Q: Identify all functional groups in the structure below. Make sure to circle and label each of them
A: A functional group is an atom or group of atoms other than the main hydrocarbon chain that is…
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- 7. How many isomers does hexane have? Draw and name them below. Discussion 1. Consider the following data table of the boiling points of alkanes. Alkanė Boiling Point (°C) Нeptane Propane Pentane 98.5 -42 36 Butane 0.5 Methane -161 Ethane -88.5 Hexane On a separate piece of graph paper, make a line graph of this data. Be sure to label the axes and give the graph a title. Based on information contained in the table, predict the approximate boiling point of hexane, and explain why.What is the name of the IUPAC compound shown here? (see attatchement) First time you guys answered it was wrong, trying again. **** The answer 3-methylbut-1-ene you gave yesterday was WRONG . Please help with correct answer. This is what the question has as well: Alkanes are called saturated hydrocarbons because each carbon atom has the maximum number of hydrogen atoms. In contrast, alkenes and alkynes are unsaturated because they contain double or triple bonds that reduce the number of hydrogen atoms in the compound. When naming unsaturated hydrocarbons, a suffix reflects the type of multiple bond in the compound: ene is used for alkenes (double bond), and yne is used for alkynes (triple bond). For cyclic alkenes and alkynes, the ring is numbered such that the double or triple bond is between the first two carbon atoms. For straight-chain molecules, the numbering starts at one end of the chain, so the location of the double or triple bond must be specified in the name.Next, let's explore what happens when you remove two hydrogens from the structure above and form ethene, CH,CH,. How many bonds should be between the two carbons to give each carbon a total of four bonds? Draw the structural formula for ethene, CH,CH,.
- Identify the functional groups in the following molecules. (Use names from the table below. List each class of functional group only once. If there are fewer than 3 functional groups, leave an appropriate number of answer boxes empty.) a) H, b) CH,CHCOH NH3 Structures of Some Common Functional Groups Name Structure Name Structure Alkene Nitro Alkyne -CC Thiol Arene Aldehydo Halide Ketone DF. C. Alcohol Carboxylic Acid Prevesus NeatHexane is an unbranched alkane with the condensed structure CH, CH,CH,CH, CH, CH, . Draw the complete structure of hexane. Show all hydrogen atoms. Select Draw Rings More // Draw the skeletal structure of hexane in line-bond (or line-angle) mode. Do not show hydrogen atoms. Draw Rings More Select C.A model of an alkane appears in the window below. ball & stick -+labels Which of the following represent structural isomers of the molecule shown in the model? Choose all that apply. CH3 CH3-CH2-CH-CH2-CH2-CH3 CH₂ CH3-CH2-CH-CH2-CH2-CH2-CH3 CH3 CH3 CH3-CH-CH-CH3 CH3 CH3-CH2-CH2-CH-CH2-CH2-CH3 CH3 CH3-CH-CH2-CH2-CH2-CH2CH3
- Examine the cycloalkane above. There are two carbons that make up the front of the ring, and three carbons that make up the back of the ring. Now, if you take the above compound, and place a METHYL group on the carbon in the frontmost right position of the ring, you will have a cycloalkane with three groups, all on different neighboring carbons. The correct complete IUPAC name for this NEW compound would be (including numbers when required): cyclopentaneA Moving to another question will save this response. estion 18 Which of the following is NOT a correct name for the alkane shown with it? (Drawing the structures wilI help!) O C7H16, heptane О С2Н6, ethane O C10H22, decane CH4, methane O C3H12. propane Moving to another question will save this response. MacBoA. Structural Isomerism of Alkanes, continued. Construct models for the five alkanes that have the molecular formula C6H₁4. All five of your models should have the same number of each type of atom, but they should have the atoms connected in a different order. Thus the molecules they represent are structural isomers of one another. Note the tetrahedral geometry of each carbon atom. Draw an extended and a condensed structure (NOT skeletal/line angle) of each structural isomer, then determine its IUPAC name. Recall that since the IUPAC name specifies the number of each type of atom and how they are connected, each structural isomer will have a different name. Each name should very specifically describe the structure. Isomer 3: Extended Structure Isomer 3: Condensed Structure IUPAC Name: IUPAC Name: Isomer 4: Extended Structure Isomer 4: Condensed Structure
- A model of an alkane appears in the window below. ball & stick ♥ Which of the following represent structural isomers of the molecule shown in the model? Choose all that apply. CH3 CH3-CH₂-C-CH₂-CH3 CH3 CH3 CH3-CH-CH₂-CH3 CH3 CH3 CH3-C -CH-CH₂-CH3 CH3 CH₂-CH3 CH3-CH2-C-CH2-CH3 中 CH3 + labels CH3 CH3-CH₂-CH-CH2-CH2-CH2CH3Identify whether the compound is an alkane, alkane, alcohol, or ether. Note: I need answers immediately. I will send a good rating right away as well.For this problem, please draw skeletal structures for the following two molecules (you will have two drawings in your answer.) Take a picture of your structures and upload it for grading. • 1-chloro-3,3-dimethylpentane 1,1-dibromo-2-methylcyclohexane