Indicate the number of signals and the multiplicity of each signal in the 1H NMR spectrum of each of the following compounds:
c. ClCH₂CH₂CH₂Cl 

Verified step by step guidance

1. Analyze the structure of the compound ClCH₂CH₂CH₂Cl. It consists of a three-carbon chain with chlorine atoms attached to the terminal carbons. This is a symmetrical molecule.
2. Determine the number of unique hydrogen environments. The terminal CH₂ groups (ClCH₂-) are equivalent due to symmetry, and the central CH₂ group (-CH₂-) is distinct. Thus, there are two unique hydrogen environments.
3. For the terminal CH₂ groups (ClCH₂-), consider the splitting pattern. Each hydrogen in this group is coupled to the two hydrogens on the adjacent central CH₂ group. This results in a triplet (n+1 rule, where n = 2).
4. For the central CH₂ group (-CH₂-), consider the splitting pattern. Each hydrogen in this group is coupled to the two hydrogens on one terminal CH₂ group and the two hydrogens on the other terminal CH₂ group. This results in a quintet (n+1 rule, where n = 4).
5. Summarize the 1H NMR spectrum: There are two signals. The terminal CH₂ groups produce a triplet, and the central CH₂ group produces a quintet.

Key Concepts

Nuclear Magnetic Resonance (NMR) Spectroscopy

NMR spectroscopy is a powerful analytical technique used to determine the structure of organic compounds. It relies on the magnetic properties of certain nuclei, primarily hydrogen (1H), to provide information about the number of hydrogen atoms in different environments within a molecule. The resulting spectrum displays signals that correspond to these environments, allowing chemists to infer structural details.

Chemical Shift

Chemical shift refers to the position of a signal in an NMR spectrum, which is influenced by the electronic environment surrounding the hydrogen atoms. Different functional groups and molecular structures can cause shifts in the resonance frequency of protons, leading to distinct signals. Understanding chemical shifts helps in identifying the types of hydrogen environments present in a compound.

Multiplicity

Multiplicity in NMR refers to the splitting of a signal into multiple peaks, which occurs due to spin-spin coupling between neighboring hydrogen atoms. The number of peaks is determined by the n+1 rule, where n is the number of adjacent protons. This information provides insight into the number of neighboring hydrogens and helps in elucidating the connectivity and arrangement of atoms in the molecule.