(a)
Interpretation: The stability of the given nuclide is to be predicted. The type of radioactivity of the unstable nuclide is to be stated.
Concept introduction: The nuclides having the neutron to proton ratio close to
To determine: The stability of the
(b)
Interpretation: The stability of the given nuclide is to be predicted. The type of radioactivity of the unstable nuclide is to be stated.
Concept introduction: The nuclides having the neutron to proton ratio close to
To determine: The stability of the
(c)
Interpretation: The stability of the given nuclide is to be predicted. The type of radioactivity of the unstable nuclide is to be stated.
Concept introduction: The nuclides having the neutron to proton ratio close to
To determine: The stability of the
(d)
Interpretation: The stability of the given nuclide is to be predicted. The type of radioactivity of the unstable nuclide is to be stated.
Concept introduction: The nuclides having the neutron to proton ratio close to
To determine: The stability of the
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Chapter 18 Solutions
Chemistry: An Atoms First Approach
- Synthesize 2-Ethyl-3-methyloxirane from dimethyl(propyl)sulfonium iodide using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize 2-Hydroxy-2-phenylacetonitrile from phenylmethanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- Synthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIf possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.arrow_forwardSynthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- Indicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forwardWe mix N-ethyl-2-hexanamine with excess methyl iodide and followed by heating with aqueous Ag2O. Indicate the major products obtained.arrow_forwardIndicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forward
- Indicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forwardIndicate the products obtained if (E)-2-butenal and 3-oxo-butanenitrile are mixed with sodium ethoxide in ethanol.arrow_forwardQuestion 3 (4 points), Draw a full arrow-pushing mechanism for the following reaction Please draw all structures clearly. Note that this intramolecular cyclization is analogous to the mechanism for halohydrin formation. COH Br + HBr Brarrow_forward
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