Concept explainers
Interpretation:
The function of the given reagent has to be identified.
Concept Introduction:
When a reagent functions as a nucleophile, substitution reaction takes place and when a reagent functions as a base, elimination reaction takes place. The first step is to determine the reagent to be strong or weak nucleophile and whether it is a strong or weak base. Basicity and nucleophilicity do not always parallel each other.
When comparing the atoms in the same row in periodic table, the basicity and nucleophilicity parallel each other. An example is,
When comparing the atoms in the same column in periodic table, the basicity and nucleophilicity do not parallel each other. An example is,
Basicity measures the charge stability on atom, while nucleophlicity measures how fast a nucleophile attacks. Basicity is a
Nucleophile (Only): This category consists of reagents that act only as strong nucleophiles and not as bases. The reagent from this category involves in substitution reaction and not elimination.
Base (Only): This category consists of reagents that act only as bases and not as nucleophiles. The reagent from this category involves in elimination reaction and not substitution.
Strong Nucleophile/Strong Base: This category consists of reagents that are strong bases and also strong nucleophiles. This includes hydroxide, alkoxide ions. Generally these reagents are used for bimolecular process.
Weak Nucleophile/Weak Base: This category consists of reagents that are weak bases and weak nucleophile. This includes reagents such as water, alcohols. Generally these reagents are used for unimolecular process.
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Chapter 10 Solutions
ORGANIC CHEMISTRY-NEXTGEN+BOX (1 SEM.)
- Q1: For each molecule, assign each stereocenter as R or S. Circle the meso compounds. Label each compound as chiral or achiral. OH HO CI Br H CI CI Br CI CI Xf x f g Br D OH Br Br H₂N R. IN Ill I -N S OMe D II H CO₂H 1/111 DuckDuckGarrow_forwardThese are synthesis questions. You need to show how the starting material can be converted into the product(s) shown. You may use any reactions we have learned. Show all the reagents you need. Show each molecule synthesized along the way and be sure to pay attention to the regiochemistry and stereochemistry preferences for each reaction. If a racemic molecule is made along the way, you need to draw both enantiomers and label the mixture as "racemic". All of the carbon atoms of the products must come from the starting material! ? H Harrow_forwardQ5: Draw every stereoisomer for 1-bromo-2-chloro-1,2-difluorocyclopentane. Clearly show stereochemistry by drawing the wedge-and-dashed bonds. Describe the relationship between each pair of the stereoisomers you have drawn.arrow_forward
- Classify each pair of molecules according to whether or not they can participate in hydrogen bonding with one another. Participate in hydrogen bonding CH3COCH3 and CH3COCH2CH3 H2O and (CH3CH2)2CO CH3COCH3 and CH₂ CHO Answer Bank Do not participate in hydrogen bonding CH3CH2OH and HCHO CH3COCH2CH3 and CH3OHarrow_forwardNonearrow_forwardQ4: Comparing (3S,4S)-3,4-dimethylhexane and (3R,4S)-3,4-dimethylhexane, which one is optically active? Briefly explain.arrow_forward
- Nonearrow_forwardNonearrow_forwardGiven the standard enthalpies of formation for the following substances, determine the reaction enthalpy for the following reaction. 4A (g) + 2B (g) → 2C (g) + 7D (g) AHrxn =?kJ Substance AH in kJ/mol A (g) - 20.42 B (g) + 32.18 C (g) - 72.51 D (g) - 17.87arrow_forward
- Determine ASran for Zn(s) + 2HCl(aq) = ZnCl2(aq) + H2(aq) given the following information: Standard Entropy Values of Various Substance Substance So (J/mol • K) 60.9 Zn(s) HCl(aq) 56.5 130.58 H2(g) Zn2+(aq) -106.5 55.10 CI (aq)arrow_forward3) Catalytic hydrogenation of the compound below produced the expected product. However, a byproduct with molecular formula C10H12O is also formed in small quantities. What is the by product?arrow_forwardWhat is the ΔHorxn of the reaction? NaOH(aq) + HCl(aq) → H2O(l) + NaCl(aq) ΔHorxn 1= ________ kJ/molarrow_forward
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