(a)
Interpretation:
Structural formula of 2-methyl-1-propanamine has to be given.
Concept introduction:
In chemistry Structure is the arrangement of
Depending on the number of carbon side chain of the amide, different types of amides can form.
From the name of the compound its structure can be determined.
Primary amines can be named in the IUPAC system in several ways,
For simple amines the suffix – amine is added to the name of the alkyl substituent.
The suffix-amine can be used in place of the final –e in the name of the parent compound.
For a secondary amine an N prefixes the compound giving the shorter carbon chain and its chain prefix name.
For a tertiary amine an N, N prefixes the compound giving the two shorter carbon chains and their side chain prefix names.
(b)
Interpretation:
Structural formula of cyclohexanamine has to be determined.
Concept introduction:
In chemistry Structure is the arrangement of chemical bonds between atoms in a molecule, specifically which atoms are chemically bonded to what other atoms with what kind of chemical bond.
Amines are the derivatives of ammonia
Depending on the number of carbon side chain of the amide, different types of amides can form.
From the name of the compound its structure can be determined.
Primary amines can be named in the IUPAC system in several ways,
For simple amines the suffix – amine is added to the name of the alkyl substituent.
The suffix-amine can be used in place of the final –e in the name of the parent compound.
For a secondary amine an N prefixes the compound giving the shorter carbon chain and its chain prefix name.
For a tertiary amine an N, N prefixes the compound giving the two shorter carbon chains and their side chain prefix names.
(c)
Interpretation:
Structural formula of (R)-2-butanamine has to be given.
Concept introduction:
In chemistry Structure is the arrangement of chemical bonds between atoms in a molecule, specifically which atoms are chemically bonded to what other atoms with what kind of chemical bond.
Amines are the derivatives of ammonia
Depending on the number of carbon side chain of the amide, different types of amides can form.
From the name of the compound its structure can be determined.
Primary amines can be named in the IUPAC system in several ways,
For simple amines the suffix – amine is added to the name of the alkyl substituent.
The suffix-amine can be used in place of the final –e in the name of the parent compound.
For a secondary amine an N prefixes the compound giving the shorter carbon chain and its chain prefix name.
For a tertiary amine an N, N prefixes the compound giving the two shorter carbon chains and their side chain prefix names.
R and S nomenclature: it is used to assign the molecule using CIP rules.
According to Cahn-Ingold-Prelog system,
The group attached to asymmetric center should be ranked based on the
Check the direction of arrow drawn in the direction of decreasing priority. If the arrow points clockwise direction, then the atom has R configuration. If the arrow points counterclockwise direction, then the atom has S configuration. If the group with lowest priority is not bonded by a hatched wedge, then interchange this group (lowest priority) by group bonded to hatched wedge and draw the arrow in priority order but the configuration is assigned as just reverse.
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ORGANIC CHEMISTRY-OWL V2 ACCESS
- Don't used Ai solutionarrow_forwardDon't used Ai solutionarrow_forward5. A solution of sucrose is fermented in a vessel until the evolution of CO2 ceases. Then, the product solution is analyzed and found to contain, 45% ethanol; 5% acetic acid; and 15% glycerin by weight. If the original charge is 500 kg, evaluate; e. The ratio of sucrose to water in the original charge (wt/wt). f. Moles of CO2 evolved. g. Maximum possible amount of ethanol that could be formed. h. Conversion efficiency. i. Per cent excess of excess reactant. Reactions: Inversion reaction: C12H22O11 + H2O →2C6H12O6 Fermentation reaction: C6H12O6 →→2C2H5OH + 2CO2 Formation of acetic acid and glycerin: C6H12O6 + C2H5OH + H₂O→ CH3COOH + 2C3H8O3arrow_forward
- Show work. don't give Ai generated solution. How many carbons and hydrogens are in the structure?arrow_forward13. (11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the molecule depicted below. Bond B 2°C. +2°C. cleavage Bond A •CH3 + 26.← Cleavage 2°C. + Bond C +3°C• CH3 2C Cleavage E 2°C. 26. weakest bond Intact molecule Strongest 3°C 20. Gund Largest argest a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in appropriate boxes. C Weakest bond A Produces Most Bond Strongest Bond Strongest Gund produces least stable radicals Weakest Stable radical b. (4pts) Consider the relative stability of all cleavage products that form when bonds A, B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B, and C are all carbon radicals. i. Which ONE cleavage product is the most stable? A condensed or bond line representation is fine. 13°C. formed in bound C cleavage ii. Which ONE cleavage product is the least stable? A condensed or bond line representation is fine. • CH3 methyl radical Formed in Gund A Cleavage c.…arrow_forwardBr. COOH Br, FCH COOH E FeBr ASOCI B NH (CH,CO),OD Br₂ 2 C alcKOHarrow_forward
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