Related Experiment Video
Updated: Jan 22, 2026

Caffeine Extraction, Enzymatic Activity and Gene Expression of Caffeine Synthase from Plant Cell Suspensions
Published on: October 2, 2018
Caffeinated Alcoholic Beverages and Intimate Partner Violence Victimization
Cory A Crane1,2, Robert C Schlauch3, Kathleen E Miller4
1Department of Biomedical Sciences, Rochester Institute of Technology, Rochester, New York.
Caffeinated alcoholic beverage (CAB) consumption is linked to increased risk of intimate partner violence (IPV) victimization for both men and women. This study provides initial evidence of this association, highlighting a potential public health concern.
Area of Science:
- Public Health
- Social Psychology
- Substance Use Research
Background:
- Caffeinated alcoholic beverage (CAB) use is linked to general victimization.
- No previous studies have investigated the association between CAB use and intimate partner violence (IPV) victimization.
Purpose of the Study:
- To examine the relationship between CAB use and IPV victimization.
- To determine if CAB use increases the risk of physical and sexual IPV.
Main Methods:
- Online survey administered to 100 respondents (40 female).
- Logistic regression analyses were used to assess the association between CAB use and IPV victimization.
- Analyses adjusted for demographic factors and heavy alcohol consumption.
Main Results:
- CAB use was significantly associated with physical and sexual IPV victimization.
- No substantial sex differences were found in the strength of the CAB use-IPV victimization relationship.
- Exploratory analyses indicated a consistent association across genders.
Conclusions:
- CAB consumption may elevate the risk of IPV victimization for both males and females.
- Findings suggest a need for further research into the specific mechanisms linking CAB use to IPV.
- Public health initiatives may need to address the risks associated with CAB consumption.
More Related Videos
Related Concept Videos
Oxidation of Alcohols
The process of oxidation in a chemical reaction is observed in any of the three forms:
Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis
Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.
Protection of Alcohols
Protection
It defines a protecting group as the masking agent to make the more reactive species inert to a given set of conditions. This concept is depicted via the illustration of liquid flow through different outlets in an assembly of pipes. The analogy helps to understand the role...
Preparation of Alcohols via Substitution Reactions
Alcohols can be synthesized from alkyl halides via nucleophilic substitution reactions. The highly polar carbon-halogen bond in the substrate makes halide a good leaving group. The hydroxide ion or water can act as a nucleophile to take the place of halide and form an alcohol. The substitution reactions occur via two different reaction pathways, SN1 or SN2, depending on the nature of carbon attached to the halide.
Primary alcohols are synthesized from primary alkyl halides, and the...
Esters to Alcohols: Hydride Reductions
Lithium aluminum hydride is a source of hydride ions and functions as a nucleophile. The mechanism proceeds in three steps. Firstly, the nucleophilic hydride ion attacks the carbonyl carbon of the ester to form a tetrahedral intermediate. Subsequently, the carbonyl group re-forms,...
Esters to Alcohols: Grignard Reaction
The reaction requires two equivalents of the Grignard reagent and introduces two identical alkyl groups, derived from the Grignard reagent, bonded to the hydroxyl-bearing carbon of the alcohol.
The reaction follows the typical nucleophilic acyl substitution mechanism. The Grignard...

