How can you distinguish E and Z isomers by nmr?

Related questions

• Why does E-Z isomerism occur?
• What is E-Z isomerism?
• Why does the E-Z notation replace the limited cis-trans notation?
• Does the energy barrier cause the existence of two distinct isomers?
• Why does IUPAC recommend NOT to use the term geometrical/geometric isomerism?
• How can I draw 1–bromo–1–chloropropene, (#CH_3CH = CBrCl#), and know if it shows E-Z isomerism?
• How can I draw 3–methylpent–2–ene, (#CH_3CH = C(CH_3) CH_2CH_3#), and know if it shows E-Z isomerism?
• What is the difference between E/Z isomerism and cis/trans isomerism?
• Why does a higher atomic number have priority in E-Z isomerism?
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