Chapter 14 9) Draw the condensed structures of two carbon organic compounds: Ethanoic acid, Ethanal (acetaldehyde)...
14. Draw Lewis structures for the following compounds. If they exhibit resonance, draw one other resonance structure for a total of two structures. b. NO a. ХеО,F, d. SO с. С.Н, f. KrF e. SCI, 15. Draw three resonance structures of NO, in which the atoms are arranged in the order NNO. Indicate the formal charges in each.
write condensed structures fore each of the following
compounds
Homework Problems 7.1 Write condensed structures for each of the following compounds: a. 2,2,4-trimethylpentane b. 5-isopropyl-2-methyloctane c. 1,1,3,3-tetrabromopropane d. 1,1-dichlorocyclopentane e. 1,4-diethylcyclohexane f. 1-bromo-2-methylcyclobutane What are the IUPAC names of the following compounds? 7.2 CH2CH, CH3 a) CH, C CH, CH, CH СH,CH, сн, CH2CH, b) CH2CH d) (CH),CCH2CH e) F Br Br Write the structural formulas and names for FOUR isomers of cycloalkane, CSH10. 7.3 7.4 Propose structures for molecules...
Draw correct. condens Cyclic portions of structures condensed structures for the following compounds according to IUPAC rules portions of structures can be done as line-angle drawings (20 pts.) b) |-ethyl-2-methylcyclohexane a) 1.1.2-trichloro-2-fluoropropane d) cis-4,4,5,5-tetramethyl-2-hexene 3-ethyl-2,2,3-trimethyloctane 3,3-dimethyl-1-octyne 4-ethyl-2-heptene 8) 1-chloro-2-propyleyelopropane h) 1,2,4-tribromo-3-chlorocyclohexane i) trans-4-ethyl-2-octene i) 1-bromo-1-chlorocycloheptane 3) hake 1-bromopentane as the only product from the reaction of 1-pentene with Can you easily make 1-bromopentane as the HBr and why? (Explain!) (10 pts.) (HINT: You may want to draw out a chemical...
A synthetic trap occurs when a reaction can give more than one desired product. For the reaction below, draw the structures of the two organiccompounds that were actually formed following the addition of \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{Li}\) and subsequent aqueous acid workup.Draw the structures of the two organic compounds which were actually isolated so that all eleven carbons involved in the reactions are accounted for in your answer.
Q.1. Draw structures and make models for the following compounds. Predict the angle(s) around each carbon atom(s) of methane and ethane. a) Methane, CH4 Angle: b) Ethane, C2H6 Angles c) Two isomers of butane, C4H10.
Draw the structures of the organic products in each reaction of the
following two-step synthesis. (Hint:
The nucleophilic amine attacks the electrophilic carbonyl carbon,
and the resulting intermediate undergoes a proton shift and
dehydration. Recall what is eliminated in a dehydration process.
The second step is a reduction reaction; the reducing agent is
NaBH3CN (or H2, metal catalyst). The aromatic ring is unaffected by
these reagents. Look at the product of the first reaction and
consider what can be easily...
Draw the structures of the organic products in each reaction of the
following two-step synthesis. (Hint:
The nucleophilic amine attacks the electrophilic carbonyl carbon,
and the resulting intermediate undergoes a proton shift and
dehydration. Recall what is eliminated in a dehydration process.
The second step is a reduction reaction; the reducing agent is
NaBH3CN (or H2, metal catalyst). The aromatic ring is unaffected by
these reagents. Look at the product of the first reaction and
consider what can be easily...
9.(1 point total, 0.5 points each) Draw two resonance structures of the conjugate base of ascorbic acid (vitamin C). HO HO
1. Draw these straightforward Lewis structures for these compounds and ions. CO2 HCCH H20 NO2 NH3 NO3 NH4+ PCI: H2CO CC14 The shape of molecules is determined primarily by the number of groupings ("electron domains") around the central atom. For the structures above there, are: Two electron domains around the central atom in CO2, HCCH Three electron domains around the central atom in H2CO, NO3-, NO2 Four electron domains around the central atom in NH3, NH4+, H20, PC13, CC14 2....