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- What functional group is at 763ppm? For HNMR at about 2.3ppm is it a quintuplet? How do I get the structure from this?Assume for the purposes of this problem that to be an alcohol (-ol) or an amine (-amine), the hydroxyl or amino group must be bonded to a tetrahedral (sp3 hybridized) carbon atom. Write the structural formula of a compound with an unbranched chain of four carbon atoms that is an: Q. Alkenoic acidAssume for the purposes of this problem that to be an alcohol (-ol) or an amine (-amine), the hydroxyl or amino group must be bonded to a tetrahedral (sp3 hybridized) carbon atom. Write the structural formula of a compound with an unbranched chain of four carbon atoms that is an: Q. Alkynoic acid
- classify the molecules of interest (i.e. para-aminophenol, acetaminophen, phenacetin) in increasing order of polarity? Rationalize these observations based on molecular interactions.Assume for the purposes of this problem that to be an alcohol (-ol) or an amine (-amine), the hydroxyl or amino group must be bonded to a tetrahedral (sp3 hybridized) carbon atom. Write the structural formula of a compound with an unbranched chain of four carbon atoms that is an: Q. AlkenamineThe compound acetophenone has a very similar molar mass to that of benzoic acid and benzamide. However, acetophenone has a much lower m.p. (20 °C) than both such that, by contrast, it is a liquid at room temperature. By considering intermolecular forces and comparing functional group structure, account for this big difference in physical properties.
- Assume for the purposes of this problem that to be an alcohol (-ol) or an amine (-amine), the hydroxyl or amino group must be bonded to a tetrahedral (sp3 hybridized) carbon atom. Write the structural formula of a compound with an unbranched chain of four carbon atoms that is an: Q. AlkenolAssume for the purposes of this problem that to be an alcohol (-ol) or an amine (-amine), the hydroxyl or amino group must be bonded to a tetrahedral (sp3 hybridized) carbon atom. Write the structural formula of a compound with an unbranched chain of four carbon atoms that is an: Q. AlkanamineAssume for the purposes of this problem that to be an alcohol (-ol) or an amine (-amine), the hydroxyl or amino group must be bonded to a tetrahedral (sp3 hybridized) carbon atom. Write the structural formula of a compound with an unbranched chain of four carbon atoms that is an: Q. Alkanone
- Assume for the purposes of this problem that to be an alcohol (-ol) or an amine (-amine), the hydroxyl or amino group must be bonded to a tetrahedral (sp3 hybridized) carbon atom. Write the structural formula of a compound with an unbranched chain of four carbon atoms that is an: Q. AlkenalAssume for the purposes of this problem that to be an alcohol (-ol) or an amine (-amine), the hydroxyl or amino group must be bonded to a tetrahedral (sp3 hybridized) carbon atom. Write the structural formula of a compound with an unbranched chain of four carbon atoms that is an: Q. AlkeneIodide ion reacts with chloromethane to displace chlorideion in a common organic substitution reaction: I⁻+CH3Cl →CH3I+Cl⁻ (a) Draw a wedge-bond structure of chloroform and indicatethe most effective direction of Iattack.(b) The analogous reaction with 2-chlorobutane [FigureP16.107(b)] results in a major change in specific rotation asmeasured by polarimetry. Explain, showing a wedge-bondstructure of the product.(c) Under different conditions, 2-chlorobutane loses Clin arate-determining step to form a planar intermediate [FigureP16.107(c)]. This cationic species reacts with HI and then losesHto form a product that exhibits no optical activity. Explain,showing a wedge-bond structure.