Structure (Skeleton) C Table 4: Naming Aromatic Hydrocarbons Name of Organic Compound Description (Common Name, Industrial/Commercial uses, Hazards if any)
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Q: b) C4H8Br2 (at least seven)
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- Classify the following compounds as E and Z structures as applicable:C5H8 has two elements of unsaturation (right?), which may indicate the presence of either double bonds or triple bonds or rings. Show all the possible structures1. What is resonance theory? State five conclusionstgan can be drawn from the theory. 2.What factors confer aromaticity to an organic molecule. 3. What are the various ways by which alkenes can be synthesized. 4. State the two main experiment that were used to establish the extra stability of the benzene molecule.
- Discuss the hybridization of carbon atoms in alkene C3H4and show the π-orbitaloverlaps.1. Based on the poster below:By referring to the structure of 1-octen-3-ol, deet, citriodiol, icaridin and IR3535,b) Convert the skeletal structures to condensed structures.Please draw the structure of psylocibin (C12H17N2O4P), with its hybridization and bond angles.
- Aromatic compounds must have a p orbital on every atom in the ring. Define this ?The following are the objective To discuss the elements or compounds determined with the help of polarography is different types of samples like food stuff, sea water, fuels, etc. To discuss the polarographic analysis of organic compounds To discuss other industrial important determinations for traces or minor constituents Give me the conclusion and thoughts for the following objectives. If possible notes is a must. Thank you so much.Carbenes (CR2) are neutral compounds with divalent carbon atoms. Propose two different ways that carbenes could exist. Provide the hybridization of each carbene carbon and predict the bond angles based on what you know about hybridization
- Identify the orbital overlaps of all of the bonds in propene (H2C CHCH3) and classify them as σ or π as appropriate.Doxorubicin, shown here, is an important chemotherapy drug used to treat avariety of cancers, including bladder cancer, breast cancer, and certain forms of leukemia. Doxorubicin works by binding to DNA in such a way that a portion of it penetrates the DNA double helix— a process called intercalation. During transcription— the process that forms RNA— portions of the DNA strands are temporarily separated for the base sequence to be read and then are reconnected. With bound doxorubicin, however, the double helix does not reform properly after the strands are separated, which disrupts replication— the process that forms an identical copy of DNA. Which portion of doxorubicin do you think intercalates into the DNA double helix, and why do you think it has little difficulty doing so?The allotrope of carbon known as fullerenes (aka "buckyballs") has a structure best described asThe allotrope of carbon known as fullerenes (aka "buckyballs") has a structure best described asThree dimensional network of carbon atoms joined by single bondsClosed cage structure with sides consisting of 5- and 6-membered rings with alternating double and single bonds.Chain of carbon atoms with alternating double and single bonds.Flat molecule consisting of fused 6-membered rings with alternating double and single bondsShapeless jumble of free carbon atoms.